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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

14101–14125 of 27736

HighFDA (Devices)·Z-1041-2024·2024-02-14
Optima Coil Neurovascular Embolization Devices Risk Foreign Emboli From Corrosion
BALT's Optima Coil neurovascular embolization devices may have corroded solder flux residue on the delivery pusher that could break off and cause foreign emboli in patient blood vessels.
Product
Neurovascular embolization device. The Optima Coil System is a series specialized coils that are inserted into the vasculature under angiographic visualization to embolize intracranial aneurysms and other vascular anomalies. The system consists of an embolization coil implant com
Category
Medical Device
Distribution
27 states
HighFDA (Devices)·Z-1009-2024·2024-02-14
Water Filter MAJ-2318 May Be Incorrectly Assembled, Risking Infection
Olympus MAJ-2318 water filters may be assembled incorrectly, allowing unfiltered tap water to contaminate reprocessed endoscopes and expose patients to infection risk.
Product
Water Filter MAJ-2318. This MAJ-2318 water filter has been designed to be used with Olympus endoscope reprocessor for prevent contamination of the rinse water. The MAJ-2318 water filter is compatible with OER-ELITE and OER-MINI.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0991-2024·2024-02-14
Flow-e Anesthesia System Model 6887900 Cybersecurity Vulnerability Recall
The Flow-e Anesthesia System model 6887900 is recalled due to a cybersecurity vulnerability that could allow remote access, denial of service, or code execution, potentially affecting anesthesia delivery safety.
Product
Flow-e Anesthesia System, model 6887900
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0984-2024·2024-02-14
Dual Articulating Headrest May Fail to Lock During Surgery
Steris Corporation is recalling Dual Articulating Headrests that may fail to lock in position during patient procedures, potentially causing patient injury. Affected units were manufactured between August and October 2023.
Product
Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0823-2024·2024-02-14
Locatelli Cheese Product Recalled for Improper Temperature Storage
Locatelli Crema Di Locatelli cheese was recalled because it was not held at appropriate temperatures. Improper holding temperatures could affect food safety by supporting spoilage and pathogen growth.
Product
LOCATELLI CREMA DI LOCATELLI 4/1.1# SUPC/ITEM # 8926
Category
Food
Distribution
3 states
HighFDA (Food)·F-0824-2024·2024-02-14
Auricchio Crema al Reggiano recalled for improper storage temperature
Greco Sidari is recalling Auricchio Crema al Reggiano cheese because the product was not held at appropriate temperatures, which could allow spoilage and pathogen growth. The recall affects 1,375 cases distributed to Ohio, New York, and Pennsylvania.
Product
AURICCHIO CREMA AL REGGIANO 4/1.1# SUPC/ITEM # 8927
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1016-2024·2024-02-14
BD antibiotic susceptibility test discs recalled for possible accuracy failures
BD BBL Sensi Disc Aztreonam test discs are recalled due to possible accuracy and quality control failures in antibiotic susceptibility testing. Failures could result in delayed diagnoses and inappropriate antibiotic selection.
Product
BD BBL Sensi Disc Aztreonam - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Numbers 231640¿and 231641.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0973-2024·2024-02-14
Ingenia 1.5T Patient Trolley Wheels May Attract to MRI Magnetic Field
Philips is recalling Ingenia 1.5T patient transportation trolleys with magnetic wheels that could be attracted to MRI magnetic fields. These wheels pose a potential hazard in MRI-equipped facilities when the trolley operates near the magnetic field.
Product
Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0861-2024·2024-02-14
Wegmans Mini Danish Recalled for Undeclared Soy Lecithin
Wegmans Food Markets recalls 9 oz 10-pack Assorted Mini Danish pastries (UPC 7789050815) because the product contains undeclared soy lecithin, which poses a risk to consumers with soy allergies.
Product
9 oz 10pk Assorted Mini Danish, bakery box with clear top (UPC 7789050815)
Category
Food
Distribution
9 states
HighFDA (Food)·F-0847-2024·2024-02-14
Potato salad recalled due to improper temperature control
Greco Sidari is recalling Resers potato salad due to improper holding temperature during distribution, risking spoilage and pathogen growth. Affected: 1375 cases in Ohio, New York, and Pennsylvania from November 26 to January 5, 2024.
Product
RESERS POTATO SALAD REGULAR 1/8# SUPC/ITEM # 0991p
Category
Food
Distribution
3 states
HighFDA (Food)·F-0825-2024·2024-02-14
Resers Red Skin Potato Salad Recall Due to Improper Temperature Storage
Greco Sidari is recalling Resers Red Skin Potato Salad because it was stored at improper temperatures that could allow pathogen growth. The product was distributed in Ohio, New York, and Pennsylvania.
Product
RESERS RED SKIN POTATO SALAD 2/8# SUPC/ITEM # 9139
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1010-2024·2024-02-14
PulseSpray Infusion System O-Ring Defect May Cause Medication Leaks
Angiodynamics is recalling PulseSpray Infusion System devices due to a manufacturing defect in the rotating adaptor O-ring that may compromise seal integrity and cause medication to leak during infusion.
Product
PulseSpray Infusion System devices including: PULSE SPRAY 5F/135/20, UPN: H787125004045, REF: 12500404; Pulse Spray 3Fx135x20, UPN: H787125004155, REF: 12500415; and PULSE SPRAY 5F/45/10, UPN: H787125004235, REF: 12500423.
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-1037-2024·2024-02-14
BD BBL Sensi Disc Piperacillin/Tazobactam Antibiotic Testing Discs Recalled for Accuracy Issues
BD BBL Sensi Disc Piperacillin/Tazobactam antibiotic susceptibility testing discs are recalled due to potential quality control and accuracy failures. These failures may cause delayed or inaccurate test results, affecting patient diagnosis and antibiotic treatment selection.
Product
BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231691 and 231692¿
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1034-2024·2024-02-14
Antibiotic Susceptibility Test Discs Recalled for Accuracy and QC Failures
Becton Dickinson is recalling BD BBL Sensi Disc Minocycline test discs due to potential accuracy and quality control failures that may cause delayed test results, missed diagnoses, or inappropriate antibiotic selection.
Product
BD BBL Sensi Disc Minocycline - 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231250 and 231251¿
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0846-2024·2024-02-14
Potato Salad Recalled for Improper Temperature Storage During Distribution
Resers Potato Salad Regular is being recalled due to improper temperature storage during distribution, which could potentially support pathogen growth. Affected cases were distributed to Ohio, New York, and Pennsylvania from November 2023 to January 2024.
Product
RESERS POTATO SALAD REGULAR 3/8# SUPC/ITEM # 0991C
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1025-2024·2024-02-14
Antibiotic susceptibility testing discs recalled for potential accuracy failures
Becton Dickinson's BD BBL Sensi Disc Cefuroxime testing discs may have accuracy, reproducibility, or quality-control failures in antibiotic susceptibility testing. This could delay diagnosis and lead to inappropriate antibiotic selection.
Product
BD BBL Sensi Disc Cefuroxime- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231621¿
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0318-2024·2024-02-14
FDA Recalls Lansoprazole Delayed-Release Capsules Due to Manufacturing Defects
The FDA is recalling Lansoprazole Delayed-Release Capsules USP 15 mg due to manufacturing defects including inadequate sealing, capsule damage, and missing product codes. Affected lot 411987 was distributed nationwide.
Product
Lansoprazole Delayed-Release Capsules USP, 15 mg, 14-count bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1030-2024·2024-02-14
BD BBL Ertapenem Susceptibility Test Discs Recalled for Accuracy Failures
BD BBL Sensi Disc Ertapenem test discs are being recalled due to reproducibility and accuracy failures that may cause diagnostic errors, delayed diagnosis, or inappropriate antibiotic selection.
Product
BD BBL Sensi Disc Ertapenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232174 and 232175¿
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1011-2024·2024-02-14
Lab testing discs recalled for potential antibiotic susceptibility testing failures
Becton Dickinson recalled 2.3 million lab testing discs used for antibiotic susceptibility testing due to potential quality control failures. These failures could lead to delayed diagnosis or inappropriate antibiotic selection.
Product
Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g, Catalog No. 231628 and 231629.¿ These discs are used for semi-quantitative in vitro susceptibility testing
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0826-2024·2024-02-14
Bellissimo Mascarpone cheese recalled due to improper temperature storage
Greco Sidari is recalling Bellissimo Mascarpone (1375 cases) distributed to OH, NY, and PA due to improper temperature storage that could allow spoilage and pathogenic growth.
Product
BELLISSIMO MASCARPONE SUPC/ITEM # 18270
Category
Food
Distribution
3 states
HighFDA (Food)·F-0849-2024·2024-02-14
Fresh mozzarella cheese recalled for improper temperature storage
Greco Sidari fresh mozzarella cheese sold in Ohio, New York, and Pennsylvania was not held at appropriate temperatures, which could affect spoilage and potentially support pathogen growth. Consumers should discard affected products or return them to the retailer.
Product
GRANDE .33OZ FRESH CILIEGINE MOZZ 1/3# SUPC/ITEM # 19134P
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1024-2024·2024-02-14
BD BBL Sensi Disc Ceftriaxone Test Discs Recalled for Susceptibility Testing Accuracy Issues
BD BBL Sensi Disc Ceftriaxone susceptibility test discs may have accuracy and quality control failures. These defects could lead to delayed diagnosis or incorrect antibiotic selection for H. influenzae infections.
Product
BD BBL Sensi Disc Ceftriaxone- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231634 and 231635¿
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0982-2024·2024-02-14
Laboratory Analyzer Software Bug Could Produce Erroneous Clinical Test Results
Beckman Coulter DxI 9000 immunoassay analyzers may produce erroneous lab results due to software bugs affecting unit conversion and result calculation. Affected devices use software version 1.16 or earlier; 128 devices worldwide are impacted.
Product
DxI 9000 Access Immunoassay Analyzer running software version 1.16 or prior,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0827-2024·2024-02-14
Bel Gioioso Cheese Recalled for Improper Storage Temperature
Bel Gioioso cheese was not held at appropriate temperatures during distribution, potentially allowing spoilage and pathogen growth. Consumers should not consume affected product.
Product
BEL GIOIOSO 12/1# EXACT COMBO SUPC/ITEM # 18304
Category
Food
Distribution
3 states
HighFDA (Food)·F-0840-2024·2024-02-14
Goat Cheese Recalled Due to Improper Temperature Storage Conditions
Greco Sidari is recalling Norpaco Sweetie Pepper Goat Cheese (1,375 cases, 1/5# units) distributed in Ohio, New York, and Pennsylvania. The cheese was not held at appropriate temperatures, which could support pathogen growth.
Product
NORPACO SWEETIE PEPPER GOAT CHEESE 1/5# SUPC/ITEM # 169956
Category
Food
Distribution
3 states

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14101–14125 of 27736