The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

Agency

Category

Minimum severity

Clear filters

24176–24200 of 26082

  • SevereFDA (Devices)·Z-0007-2022·2021-10-20

    Abbott Alinity m SARS-CoV-2 Test Kit Recalled for Potential False Positives

    Abbott Molecular recalls its Alinity m SARS-CoV-2 Amp Kit (Non-US Assay), an in vitro diagnostic test, due to potential for false positive results. Approximately 11,408 units were distributed worldwide.

    Product
    Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0009-2022·2021-10-20

    Glucagon Emergency Kit Recall: Subpotent Drug in Vials

    Eli Lilly is recalling Glucagon Emergency Kits (Lot #D239382D, expiration April 2022) because some vials contain liquid instead of powder and do not deliver the full expected drug effect when administered.

    Product
    Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe. Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285; Glucagon, NDC: 0002-8031-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0068-2022·2021-10-20

    Ultrasound gel products recalled for potential bacterial contamination

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. Products distributed nationwide in the U.S., Canada, and other locations have been recalled.

    Product
    ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0007-2022·2021-10-20

    Potassium Chloride Injection Recall Due to Sterility Assurance Lack

    SSM Health Care St. Louis is recalling 385 bags of Potassium Chloride 40 mEq in 0.9% Sodium Chloride injection due to lack of assurance of sterility. The affected lot was distributed in Missouri.

    Product
    Potassium Chloride 40 mEq in 0.9% Sodium Chloride 270 mL NS, 250 mL bag, Rx Only, SSM Health Care Corporation, 1015 Bowles, Fenton, MO. NDC 60652-6429-1
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0089-2022·2021-10-20

    FDA recalls Eco-Med ultrasound gels due to bacterial contamination risk

    FDA recalls ultrasound gels manufactured by Eco-Med Pharmaceutical due to possible bacterial contamination. Healthcare providers and facilities should stop use immediately.

    Product
    EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel, Model No. 250UG-CMU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0015-2022·2021-10-20

    Frozen vegan crabcakes recalled for undeclared egg allergen

    Cuisine Innovations Unlimited, LLC is recalling Vemondo Vegan Crabless Mini Crabcakes sold at Lidl due to undeclared egg. The product may pose a risk to consumers with egg allergies.

    Product
    Vemondo Vegan Crabless Mini Crabcakes by Lidl 8.5 OUNCES (240g) coated paper box ten (10) packages per case. Frozen.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0096-2022·2021-10-20

    Smiths Medical LogiCal Blood Sampling Sets Recalled for Pressure Reading Errors

    Smiths Medical ASD Inc. is recalling 870 units of LogiCal blood sampling sets distributed across Europe and Saudi Arabia due to reported pressure shifts and incorrect pressure readings.

    Product
    smiths medical medex CBSS 5 ml, dreifach proximaler Entnahmeport 60 cm, Model number DPSHC0082
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0105-2022·2021-10-20

    Thoraguard Chest Tube Kit 20 Fr Recalled for Adhesive Joint Failure

    Centese Inc. is recalling Thoraguard Chest Tube Kits (20 Fr) because an adhesive joint in the SmartValve component can fail, causing fluid to leak. The affected kits were distributed to a single facility in California.

    Product
    Thoraguard Chest Tube Kit, 20 Fr
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0093-2022·2021-10-20

    Smiths Medical HemoDraw Plus Blood Sampling Sets Recalled for Pressure Monitoring Errors

    Smiths Medical ASD Inc. is recalling 140 HemoDraw Plus Closed Blood Sampling Sets with LogiCal Pressure Monitoring System for pressure shifts and incorrect pressure readings. Affected units were distributed to Austria, France, Germany, Great Britain, and Saudi Arabia.

    Product
    smiths medical medex HemoDraw Plus Closed Blood Sampling Set with LogiCal Pressure Monitoring System, Model Numbers: a) MX961H182P1 b) MX961H212P1 c) MX962H182P1 d) MX962H212P1
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0013-2022·2021-10-20

    Curly Parsley Recalled Due to Potential STEC Contamination

    Dole Fresh Vegetables is recalling curly parsley distributed to five U.S. states due to potential non-O157 STEC (Shiga-Toxin 1) contamination. Consumers should not consume the affected product.

    Product
    Bunches of curly parsley packed in cardboard cases received at distributor level with following labeling: Herb Parsley Curly Grown in Salinas 60EA x 60EA Bunch US or 30EA x 60EA Bunch US Dole Fresh Vegetables, Monterey, CA 93940 PLU 4899 0 07143 00310 Harvest Date Aug18 Bunches
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0100-2022·2021-10-20

    Smiths Medical Antishunt Sets Recalled Due to Pressure and Reading Errors

    Smiths Medical ASD Inc. is recalling approximately 20,800 Antishunt blood sampling sets due to reported pressure shifts and incorrect pressure readings. The affected model was distributed in Austria, France, Germany, Great Britain, and Saudi Arabia.

    Product
    smiths medical medex CBSS-5ML Antishunt set, (172/15cm), Model Number DPSHC0091
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0109-2022·2021-10-20

    Babylog VN500 Ventilator Firmware Defect May Cause Brief Ventilation Interruption

    A software defect in the Babylog VN500 Ventilator may cause it to restart, interrupting ventilation and losing PEEP for about 8 seconds. The issue affects 2,169 units distributed nationwide.

    Product
    Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for the ventilation of neonatal patients from 0.4 kg (0.88 lbs) up to 10 kg (22 lbs) and pediatric patients from 5 kg (11 lbs) up to 20 kg (44 lbs) bodyweight. Catalog Number: 8417400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V825000·2021-10-20

    2021-2022 Audi vehicles recalled for rear-view camera software failure

    Volkswagen Group is recalling certain 2021-2022 Audi vehicles due to a software error that may prevent the rear-view camera from displaying when reversing, potentially reducing driver visibility and increasing crash risk.

    Product
    AUDI — 2021 AUDI A8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0083-2022·2021-10-20

    Cobas EGFR Mutation Test v2 may return false mutation detection results

    The cobas EGFR Mutation Test v2 may produce false positive results for exon 20 insertion mutations, potentially leading to inappropriate treatment. Healthcare providers should verify detected mutations using alternative methods.

    Product
    cobas EGFR Mutation Test v2-Somatic gene mutation detection system Catalog Number :07248563190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0094-2022·2021-10-20

    Smiths Medical blood sampling system recalled for pressure measurement errors

    Smiths Medical is recalling 3,100 units of its CBSS blood sampling system due to pressure measurement failures. The devices may show incorrect pressure readings or experience pressure shifts during use.

    Product
    smiths medical medex CBSS 2-fach Druckmesset mit Option, Model Number DPSHC0076
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0087-2022·2021-10-20

    Automation System Interface Module Firmware May Misassociate Test Results to Samples

    Inpeco's automation interface module firmware may incorrectly associate laboratory test results with patient sample IDs, potentially causing incorrect patient results.

    Product
    FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2). (Different brand names of same product.)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0016-2022·2021-10-20

    Litehouse Ranch Dressing Recall for Undeclared Anchovies

    Litehouse Inc. is recalling Ranch dressing packaged in 1.25 oz. plastic cups because the product contains undeclared anchovies, a potential allergen not listed on packaging.

    Product
    Litehouse item 15533 Ranch dressing packaged in 1.25 oz. plastic cup with seal, 336 cups per case. It is printed on the side of a plastic cup as 1231 1.25 OZ 02 83027 15533 RANCH. These cups are un-labeled and not intended for sale as individual cup at retail stores. The master
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0079-2022·2021-10-20

    Philips Defibrillators Recall: Customers Uninformed of Previous Recalls

    Customers of Philips HeartStart FRx defibrillators were not notified of previous recalls associated with various defibrillator models. This is a Class II medical device recall.

    Product
    Philips, HeartStart FRx + Defibrillator, Model # Model #s: 861304
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Devices)·Z-0112-2022·2021-10-20

    Flower Drill Bit Kit 2.4mm missing AO connect feature

    Flower Orthopedics Corporation is recalling 33 units of its 2.4mm Drill Bit Kit (Lot 2101321194) because the drill bits lack the AO connect feature, which may delay surgical procedures.

    Product
    Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can be used with any plate as part of the Flower Small and Medium Implant Set and uses the small locking mechanism. Catalog Number: DBK 024
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0110-2022·2021-10-20

    United Orthopedics USTAR II knee implant component recalled for specification failures

    Uoc Usa Inc recalls 3 United Orthopedics USTAR II knee components that fail to meet manufacturing specifications for concentricity and dynamic fatigue testing. These defects could affect implant performance.

    Product
    United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 mm Length, Catalog # 2915-1025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0104-2022·2021-10-20

    K2M Surgical Removal Tool Recalled for Missing Pins

    K2M, Inc. is recalling 23 units of the Chesapeake Anterior Lumbar Removal Tool because units may arrive with missing pins or in disassembled condition. Pins could dislodge during surgery and enter the surgical cavity, requiring intraoperative removal or revision surgery.

    Product
    Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0082-2022·2021-10-20

    Bio-Rad BioPlex 2200 ANA Screen Control lot incompatible with reagents

    Bio-Rad Laboratories has recalled certain lots of BioPlex 2200 ANA Screen Control Sets due to incompatibility with older lots of ANA Screen Reagent Packs and Calibrator Sets, which may affect test accuracy.

    Product
    BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with ANA Screen Reagent Packs/ANA Kits, REF: 665-1150; and ANA Screen Calibrator Sets, REF: 663-1101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0098-2022·2021-10-20

    Medical Device Recall: Blood Sampling System Pressure and Reading Errors

    Smiths Medical is recalling LogiCal Closed Blood Sampling System sets due to reported pressure shifts and incorrect pressure readings that could affect blood collection accuracy.

    Product
    smiths medical medex CBSS 5 ml, zweifach proximaler Entnahmeport 60 cm, Model Number DPSHC0084
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0092-2022·2021-10-20

    Medex LogiCal Closed Blood Sampling System Recalled for Pressure Reading Errors

    Smiths Medical ASD Inc. is recalling medex LogiCal 5mL Closed Blood Sampling System sets due to reported pressure shifts and incorrect pressure readings that could affect patient safety.

    Product
    medex LogiCal 5mL Closed Blood Sampling System, Model Numbers: a) MX961E181P1 b) MX961E211P1 c) MX962E211P1 d) MX96AE181P1 e) MX96AE211P1
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0117-2022·2021-10-20

    Beckman Coulter Power Processor 3K Recalled for Missing Splash Guard

    Beckman Coulter is recalling Power Processor 3K laboratory equipment due to a missing splash guard that may expose users to hazardous materials. Approximately 271 units were distributed in the U.S. and internationally.

    Product
    Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A88116
    Category
    Medical Device
    Distribution
    Distributed nationwide