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.

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17826–17850 of 27833

  • HighFDA (Devices)·Z-2006-2023·2023-07-05

    Voalte Patient Safety software may fail to alert caregivers of safety changes

    Baxter's Voalte Patient Safety software may permanently stop sending caregiver alerts for critical patient protocols like bed exit and siderail changes. Affected versions V4.0.000 through V4.0.401 are used with Centrella Beds.

    Product
    Voalte Patient Safety, Part Number 4.0, V4.0.000 to 4.0.401, used with the Centrella Bed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2043-2023·2023-07-05

    Access Hybritech p2PSA Reagent Recalled for Insufficient Blocking Reagent

    Beckman Coulter is recalling Access Hybritech p2PSA diagnostic reagent kits with insufficient blocking reagent concentration. Three lot numbers affecting 987 kits were distributed in the US and internationally.

    Product
    Access Hybritech p2PSA reagent, REF B03704 and REF A49752.
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Food)·F-1301-2023·2023-07-05

    Sun Wave Brand Jelly Cups Recalled Due to Potential Choking Hazard

    Richin Trading Inc is recalling Sun Wave Brand Jelly Cups (Lychee Flavor) with multiple lot numbers due to a potential choking hazard. The recall affects 141,192 units distributed across 17 U.S. states.

    Product
    Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC 715685121529; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12145; UPC 715685121451; Net Weight 52.91 oz. (1500 g)
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-2010-2023·2023-07-05

    Limacorporate Prima TT Orthopedic Baseplate Recalled for Manufacturing Defect

    Limacorporate is recalling 13 units of the Prima TT Genoid Modular Reverse TT Baseplate due to a manufacturing issue that may cause peripheral holes to be out of specification. Healthcare facilities should contact the manufacturer.

    Product
    REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0879-2023·2023-07-05

    Endometrin Vaginal Inserts Recalled Due to Potential Microbial Contamination

    Ferring Pharmaceuticals is recalling certain lots of Endometrin (progesterone) Vaginal Inserts due to potential microbial contamination resulting from manufacturing deviations.

    Product
    Endometrin (progesterone) Vaginal Insert 100mg, packaged in a carton of 21 vaginal inserts with 21 disposable vaginal applicators, Manufactured for: Ferring Pharmaceuticals Inc., Parsippany, NJ NDC# 55566-6500-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2050-2023·2023-07-05

    Exactech Shoulder GPS Impactor Handle Recalled for Locking Mechanism Defect

    Exactech is recalling 250 units of its Shoulder GPS Impactor Handle due to a defect where the ball and spring in the locking mechanism can dislodge during disassembly or impaction. The defect could affect the device's function during surgical use.

    Product
    Exactech Shoulder GPS Impactor Handle, Catalog #531-07-05.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-2003-2023·2023-07-05

    Design Options Epidural Anesthesia Kit Recalled for Incorrect Filter Straw

    B. Braun Medical is recalling Design Options Epidural Anesthesia Kits because certain units were assembled with an incorrect filter straw. The recall affects approximately 3,560 kits distributed nationwide.

    Product
    Design Options¿ / Epidural anesthesia kit (10 count carton)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2023-2023·2023-07-05

    Verigene nucleic acid test kits recalled for rare false-negative results

    Luminex Corporation recalls Verigene nucleic acid test kits that may rarely produce false-negative results due to hydrophobic properties in certain FLOQSwab lots. False-negative results could fail to detect enteric pathogens in patient samples.

    Product
    Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2046-2023·2023-07-05

    Knee Prosthesis System Components Recalled for Specification Non-Compliance

    Waldemar Link GmbH & Co. KG is recalling 21 units of LINK Endo-Model Modular Knee Prosthesis System Femoral Segment components because they may not meet manufacturing specifications. No injuries have been reported.

    Product
    LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2047-2023·2023-07-05

    Knee Prosthesis Femoral Segment Recalled Due to Specification Compliance Issue

    Waldemar Link is recalling 22 units of the LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left, because device segments may not meet specifications. The company discovered the issue through customer complaints.

    Product
    LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-1971-2023·2023-07-05

    Integre Pro Laser Ophthalmoscope Systems: Risk of Unintended Laser Emission

    Ellex Medical is recalling certain Integre Pro laser ophthalmoscope systems because scattered laser radiation may unintentionally exit the device and be emitted from the objective lens, potentially exposing users' eyes to unexpected laser energy.

    Product
    Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green LP5532 Spare, Optics Bench V2, L2G/LP6G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2038-2023·2023-07-05

    Remel Haemophilus Test Medium Agar Packages Recalled for Performance Failure

    Remel is recalling specific lot numbers of Haemophilus Test Medium (Agar) because the test medium may not perform as intended. This diagnostic device is used in laboratory testing nationwide.

    Product
    Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In Vitro Diagnostic Use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2037-2023·2023-07-05

    Dental Implant Abutments Recalled Due to Lack of FDA Clearance

    Implant Direct Sybron is recalling LEGACY SMARTBASE dental abutments distributed without FDA clearance. Performance characteristics have not been adequately established.

    Product
    LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE; LEGACY SMARTBASE, NE 3.0D 2MML, REF 8730-82NE; LEGACY SMARTBASE NARROW NE 3.5D, REF: 8735-80NNE; LEGACY SMARTBASE, NE 3.5D 2MML, REF: 8735-82NE LEGACY SMARTBASE NARROW NE 4.5D, REF: 8745-80NNE; LEGACY SMARTBASE. NE 4.5D, REF: 8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2007-2023·2023-07-05

    NaviCare Patient Safety software versions recalled for alert suppression defect

    Baxter Healthcare is recalling NaviCare Patient Safety software for Centrella Bed. A software defect may prevent caregiver alerts for patient bed exits and positioning changes.

    Product
    NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2025-2023·2023-07-05

    Philips Respironics V60 Ventilator recalled for potential gas pathway contamination

    DRE Medical Group recalled 22 Philips Respironics V60 ventilators due to potential contamination in the gas pathway of retrofitted units. These devices may pose a serious health risk to patients.

    Product
    Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Model Number: R1053618 and R1076709. These are retrofitted device.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2020-2023·2023-07-05

    Orthopedic assembly screws with incorrect model number labeling and markings

    AEQUALIS FLEX REVIVE assembly screws were mislabeled during manufacturing, with some units marked as 0mm Standard actually being 0mm Short and vice versa. Surgeons must verify model numbers before use.

    Product
    AEQUALIS FLEX REVIVE Assembly Screw 0mm Short, Model Number ARS655118
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2036-2023·2023-07-05

    Vanta Implantable Neurostimulator May Become Unresponsive During Cardioversion

    Cardioversion procedures can damage electronics in Vanta implantable neurostimulators, making them unresponsive. Medtronic has received two complaints resulting in device removal surgeries.

    Product
    Vanta with AdaptiveStim Implantable Neurostimulator, Model 977006; spinal chord stimulation
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·23V255000·2023-07-04

    Volvo VNR Trucks Recalled for Aggressive Adaptive Cruise Control Braking

    Volvo Trucks is recalling 2020-2023 VNR Electric vehicles equipped with Adaptive Cruise Control that can trigger aggressive braking under light load conditions, risking rear axle skidding and loss of vehicle control.

    Product
    VOLVO — 2021 VOLVO VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V258000·2023-07-04

    2023 Subaru Ascent Tire Bead Damage Increases Crash Risk

    Subaru is recalling certain 2023 Ascent vehicles equipped with 20-inch wheels due to potential tire bead damage during manufacturing. The defect may cause sudden air pressure loss and increase crash risk.

    Product
    SUBARU — 2023 SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V151000·2023-07-03

    2023 Grand Design Imagine Travel Trailers Recalled for Incorrect Tire Specification Label

    Grand Design is recalling 139 units of 2023 Imagine travel trailers. The Federal Certification Label incorrectly states tire size and inflation pressure, which may cause premature tire wear or blowout, increasing crash risk.

    Product
    GRAND DESIGN — 2023 GRAND DESIGN IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V225000·2023-07-03

    Harley-Davidson motorcycles recalled for faulty headlight bulbs and visibility loss

    Harley-Davidson is recalling 2019-2021 Sportster motorcycles and replacement headlight assemblies because the glass bulb may fail, causing loss of both high and low beams and increasing crash risk.

    Product
    HARLEY-DAVIDSON — 2020 HARLEY-DAVIDSON XL1200NS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V149000·2023-07-03

    Kia K5 side curtain air bags may not deploy in crash

    Kia is recalling 2021-2023 K5 vehicles due to potentially incorrect installation of side curtain air bags that could prevent proper deployment in a crash.

    Product
    KIA — 2022 KIA K5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V224000·2023-07-03

    2021 Porsche Macan recalled for loose shock absorber screw connections

    Certain 2021 Porsche Macan models have improperly tightened screw connections on shock absorbers, which could compromise braking and vehicle control. Porsche will repair the connections free of charge.

    Product
    PORSCHE — 2021 PORSCHE MACAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23237·2023-06-29

    CaTeam Canvas Baby Hammock Swings Recalled for Suffocation Hazard

    CaTeam is recalling about 700 Canvas Baby Hammock Swings sold online from November 2022 through January 2023 because they violate the Safe Sleep for Babies Act. The inclined design poses a suffocation risk to infants.

    Product
    Canvas Baby Hammock Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23234·2023-06-29

    Bose Acoustimass, Lifestyle, and Companion Bass Modules Due to Fire Hazard

    Bose Corporation is recalling select bass modules manufactured before April 2006 because electrical components can fail and cause fires. The firm has received 21 reports of ignition or melting worldwide, with three resulting in property damage.

    Product
    Bose Acoustimass, Lifestyle and Companion bass modules (produced before April 2006)
    Category
    Consumer Product
    Distribution
    Distributed nationwide