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 the agency’s own highest classification or reported deaths or serious injuries, 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

23726–23750 of 90106

HighFDA (Devices)·Z-1669-2022·2022-09-07
Boston Scientific ZOOM LATITUDE Programmer Software Anomaly Recall
Boston Scientific is recalling ZOOM LATITUDE programmers due to potential software anomalies that could affect communication with implantable defibrillators. No injuries have been reported.
Product
The Programmer/Recorder/Monitor (PRM) is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. The software in use controls all communication functions for the pulse generator.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1671-2022·2022-09-07
Boston Scientific ZOOM LATITUDE Programmer Software Anomaly Recall
Boston Scientific ZOOM LATITUDE programmer software may have anomalies when communicating with certain Boston Scientific defibrillators, potentially affecting device programming and communication functions.
Product
The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. The software in use controls all communication functions for the pulse generator.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1652-2022·2022-09-07
RT-PCR Kit Recalled Due to False Positive Test Results
Qiagen's FGFR RGQ RT-PCR Kit may produce false positive results, leading to incorrect lab reports. This could expose cancer patients to inappropriate or suboptimal treatment.
Product
FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010
Category
Medical Device
Distribution
4 states
HighFDA (Food)·F-1581-2022·2022-09-07
Arborio Rice Recalled for Possible Glass Contamination
Multiple Arborio rice products are being recalled by Woodland Foods LLC due to possible presence of glass pieces. Consumers should not use the affected products.
Product
Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice, 25 lbs. bag UPC 00687080069143 Sysco International X06D05 Arborio Rice, 25 lbs. bag in box UPC 00074865718257 DGourmet.com X06C Arborio Rice, 10 lbs. bag in…
Category
Food
Distribution
23 states
HighFDA (Food)·F-1684-2022·2022-09-07
Clinical Innovations Sweetums Sucrose Solution Vials Recalled for Contamination
Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to complaints of leaking, black liquid, and black particulates in product vials. The recall affects neonatal products distributed nationwide and internationally.
Product
Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1645-2022·2022-09-07
X-Ray Imaging System X-Ray Tube Hardware Defect Worldwide Recall
Siemens has recalled Artis Q and Artis Q.zen X-ray imaging systems due to a potential X-ray tube hardware defect. In rare cases, if error detection fails, the system will not be able to release X-ray until shut down; 1,389 units are affected globally.
Product
Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis Q.zen floor- Model No. 10848353 Artis Q.zen ceiling- Model No. 10848354 Artis Q.zen biplane- Model No. 10848355
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1677-2022·2022-09-07
ERG! Energy Apricot P'Butter bar recalled for undeclared oats
ERG Foods is recalling ERG! Energy Apricot P'Butter Fruit and Nut Bars due to undeclared oats. The product may pose a risk to consumers with oat allergies.
Product
ERG! Energy Apricot P'Butter Fruit and Nut Bar 2.05oz. individually packaged in clear plastic, UPC Number 863444000421
Category
Food
Distribution
0 states
HighFDA (Food)·F-1681-2022·2022-09-07
Priyems Mango Pickles recalled for undeclared wheat starch
Yem Foods LLC is recalling Priyems Mango Pickles (1lb/454g) due to undeclared wheat starch from asafoetida. Consumers with wheat allergies may be at risk.
Product
Priyems Mango Pickles 1lb/454g UPC 8 61754 000179, 10 retail units per wholesale case, Refrigerated
Category
Food
Distribution
15 states
HighFDA (Devices)·Z-1651-2022·2022-09-07
therascreen FGFR RGQ Kit Recalled for Increased False Positive Results
Qiagen's therascreen FGFR RGQ RT-PCR Kit is being recalled for increased false positive results in 29 distributed kits. False positives could lead to incorrect lab reports and inappropriate cancer treatment for patients.
Product
therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-1672-2022·2022-09-07
Medical device software error affects toric IOL surgical planning accuracy
A software defect in the Pentacam AXL Wave eye imaging device's IOL calculator may inaccurately reflect alignment axis and incision position for toric lens surgeries. This affects 21 systems distributed across the U.S.
Product
Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
Category
Medical Device
Distribution
37 states
HighFDA (Drugs)·D-1468-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste Recalled for Improper Storage Conditions
Family Dollar is recalling Colgate OPTIC WHITE CHARCOAL COOL MINT toothpaste (Net Weight 4.2 oz., UPC 0 35000 97872 1) distributed to stores in 11 states due to improper temperature storage during manufacturing.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1667-2022·2022-09-07
Hip Implant Stem Recalled for Failed Fatigue Testing
Corin Ltd is recalling a hip implant stem component (Model 588.3800) after some units failed fatigue testing. The affected devices were distributed to New Jersey only.
Product
TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1641-2022·2022-09-07
TB Diagnostic Test Recalled Due to Storage Temperature Excursion
Oxford Immunotec recalled 81 T-SPOT.TB diagnostic test kits (Lot TEC4000098) due to storage equipment failure that kept products outside the validated 2-8°C temperature range. The excursion may affect test accuracy.
Product
T-SPOT.TB REF TB.300 US
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-1674-2022·2022-09-07
Pentacam HR Medical Device Software Error Impacts Surgical Planning
A software error in the Pentacam HR eye imaging device causes inaccurate IOL calculator output for toric intraocular lens surgical planning. Nineteen systems are affected.
Product
Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1644-2022·2022-09-07
Medtronic EverFlex Peripheral Stents Recalled for Partial Deployment Risk
Medtronic is recalling EverFlex peripheral stents worldwide due to risk of partial deployment. Updated instructions provide a manual deployment workaround to mitigate potential harms.
Product
EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System
Category
Medical Device
Distribution
0 states
HighNHTSA·22V670000·2022-09-07
BMW X7 Third-Row Seat Backrest Springs May Not Lock Properly
BMW is recalling 2019-2022 X7 models with third-row seats because compression springs may not have been properly installed, causing the seat backrest to potentially fail to lock in a crash.
Product
BMW — BMW X7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2022·2022-09-07
Philips Radiography System Firmware Defect Risks Incorrect Radiation Dose
Philips DigitalDiagnost C50 1.1 radiography systems contain a firmware defect in the Wallstand VS2 board that may cause incorrect radiation dose and anatomic marker misalignment. Eleven affected systems were distributed nationwide.
Product
DigitalDiagnost C50 1.1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1685-2022·2022-09-07
Sucrose solution vials recalled nationwide for contamination and leaking
Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to reports of leaking containers and contamination with black liquid and particulates. The product is used in hospital settings including neonatal intensive care units.
Product
Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1639-2022·2022-09-07
AggreGuide A-100 Instrument Software Issue Affecting Test Results
Aggredyne, Inc. is recalling the AggreGuide A-100 Instrument due to a software design defect that causes the device to run assays at 0 RPM, resulting in no blood mixing and inaccurate test results displayed as Low.
Product
AggreGuide A-100 Instrument
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1642-2022·2022-09-07
T-Cell Xtend Test Kit Recalled Due to Improper Storage Temperature
Oxford Immunotec is recalling 47 units of the T-Cell Xtend REF TTK.610 US test kit due to equipment failure that caused improper storage temperatures outside the validated range. Affected devices may have been compromised.
Product
T-Cell Xtend REF TTK.610 US
Category
Medical Device
Distribution
7 states
HighFDA (Drugs)·D-1465-2022·2022-09-07
Colgate OPTIC WHITE PRO Series Toothpaste Recalled for Improper Storage
Family Dollar Stores is recalling 1,120 packages of Colgate OPTIC WHITE PRO SERIES toothpaste due to improper temperature storage conditions that deviate from cGMP standards.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0 35000 99658 9. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1473-2022·2022-09-07
Prescription Antibiotic Tablets Recalled for Foreign Matter in Active Ingredient
Teva Pharmaceuticals is recalling Neomycin Sulfate Tablets because teflon was found in the active ingredient. Affected lot numbers: 3007830, 3007746, 3007829.
Product
NEOMYCIN SULFATE — NEOMYCIN SULFATE (NEOMYCIN SULFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1638-2022·2022-09-07
Aesculap ENNOVATE Spine Implants Recalled for Incorrect Screw Inclusion
Aesculap Implant Systems LLC recalls ENNOVATE SET SCREW spine implants because packages may contain incorrect screws. Six units distributed in Georgia and Texas.
Product
Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar, thoracic and sacral spine. Article Number: 52758014
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-1683-2022·2022-09-07
Great Value Chopped Walnuts Recalled Due to Pecan Mislabeling
Great Value Chopped Walnuts pouches containing pecans have been recalled from Walmart distribution centers in North Carolina and Florida. The product was mislabeled, which may affect consumers with nut allergies.
Product
Great Value Chopped Walnuts, NET WT 4oz (113g); Ingredients: Walnuts DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716; UPC 0 78742 20134 4
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1650-2022·2022-09-07
FGFR cancer diagnostic kit recalled due to increased false positive results
Qiagen Sciences is recalling therascreen FGFR RT-PCR kits due to increased false positive rates. False results could lead patients to receive unnecessary cancer treatment.
Product
therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721
Category
Medical Device
Distribution
4 states

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23726–23750 of 90106