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

19276–19300 of 27466

HighFDA (Devices)·Z-1149-2023·2023-03-01
Siemens Atellica IM Folate 140 test kit recalled for measurement bias
Siemens is recalling the Atellica IM Folate 140 test kit due to negative bias that occurs when whole blood calibration is mistakenly used to test serum samples, potentially producing falsely low folate measurements.
Product
Atellica IM Folate 140 test kit- For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10995572
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0338-2023·2023-03-01
Thyroid Medication TIROSINT Levothyroxine Sodium Nationwide Recall for Subpotency
IBSA Pharma Inc. is recalling TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotency. Two lot numbers are affected: Lot #220407 (Exp. 10/2023) and Lot #220960 (Exp. 03/2024).
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0341-2023·2023-03-01
Thyroid Drug TIROSINT Recalled Due to Subpotent Formulation
IBSA Pharma Inc. recalls TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotent formulation containing less active ingredient than labeled.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0334-2023·2023-03-01
Levothyroxine oral solution TIROSINT recalled nationwide for subpotency
IBSA Pharma voluntarily recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency concerns. Affected lots are 220416 (Exp. 10/2023) and 221053 (Exp. 4/2024).
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0348-2023·2023-03-01
Warfarin Sodium Tablets Recalled Due to Failed Impurity and Degradation Specifications
Rising Pharmaceuticals is recalling Warfarin Sodium Tablets USP 1 mg due to failed impurities and degradation specifications. Approximately 12,216 bottles may have been distributed nationwide.
Product
Warfarin Sodium Tablets, USP 1 mg, 100-count bottle, Rx Only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC# 57237-119-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1152-2023·2023-03-01
Diagnostic folate test kits recalled for negative measurement bias
Siemens ADVIA Centaur Folate 100 test kits are recalled due to negative bias when whole blood calibration is used to test serum samples. The affected kits may produce falsely low folate results.
Product
ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10310308
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0403-2023·2023-03-01
Cayenne Pepper Recalled for Elevated Aflatoxin Contamination
Tampico Spice Company Inc is recalling Cayenne Pepper in 1-pound and 5-pound jars due to elevated aflatoxin levels. The affected lot is #2112245, distributed across eight states.
Product
Cayenne Pepper 1 pound jars, and 5 pound jars
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1159-2023·2023-03-01
IV Start Kit Recalled Due to Connector Manufacturing Defect
Cardinal Health Presource Packs IV start kits with ICU MicroClave Clear Connectors are being recalled due to a manufacturing defect that may cause fluid leaks and loss of fluid path integrity.
Product
Cardinal Health Presource Packs IV START KIT-Intended for IV Access CATALOG #: 01A4553E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0405-2023·2023-03-01
Taco Meat Seasoning recalled for elevated aflatoxin contamination
Tampico Spice Company is recalling Taco Meat Seasoning due to elevated aflatoxin levels. Affected products in multiple sizes were distributed across eight states.
Product
Taco Meat Seasoning 1 OZ, 1 LB, 1.5 LBS, 2 LBS, 5 LBS, 6 LBS
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1168-2023·2023-03-01
Diagnostic imaging system recalled due to ceiling and wall collision risk
Siemens Uroskop Omnia Max imaging systems are recalled due to collision risk with ceilings, walls, or objects caused by default configuration settings. The systems may move dangerously, potentially injuring staff or patients.
Product
Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762473
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1150-2023·2023-03-01
Siemens Atellica IM Folate 700 test kit recalled for measurement bias
Siemens Healthcare is recalling 9,272 Atellica IM Folate 700 test kits due to negative bias in results when whole blood calibration is used to test serum samples.
Product
Atellica IM Folate 700 test kit- For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10995573
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1144-2023·2023-03-01
Hologic Mammography Systems Recalled for Unexpected C-Arm Movement
Hologic is recalling 797 units of its 3Dimensions/Selenia Dimensions mammography systems nationwide due to unexpected C-arm movement that may cause blunt trauma.
Product
Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D SDM-00001-3D SDM-05000-3D3 SDM-05000-2DC SDM-00001-M3D SDM-05000-3DC SDM-SYS-6000-3D SDM-05000-2D3 SDA-SYS-3000-2D SDM-00001 SDM-SYS-9000-2D SDM-00001-M2D 3DM-SYS-STD 3DM-SYS-STD-NS SDM-
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0345-2023·2023-03-01
Prescription Levothyroxine Sodium Oral Solution Nationwide Recall Due to Subpotency
IBSA Pharma has recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency. Affected lots 220418 and 220560 may contain insufficient active ingredient for proper thyroid hormone replacement therapy.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V134000·2023-03-01
Airstream travel trailers recalled for cooktop gas leak fire risk
Airstream is recalling 2021-2023 travel trailers with SDS2 cooktops. Burner tubes may fracture and cause gas leaks, increasing fire risk. Dealers will install a support bracket at no charge.
Product
AIRSTREAM — 2022 AIRSTREAM INTERSTATE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1143-2023·2023-03-01
Hepatitis B Diagnostic Test Kits Recalled for Test Interference
Siemens is recalling ADVIA Centaur diagnostic test kits used to detect hepatitis B antibodies due to test interference that can produce false positive results when performed before another hepatitis B test on the same sample.
Product
ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- In vitro diagnostic immunoassay for the qualitative detection of antibodies to the e antigen of the hepatitis B virus (HBV) in human pediatric (2-21 years old) and adult serum, EDTA plasma, or lithium heparin. Siemens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0360-2023·2023-03-01
Pilgrim's Roasted Nut'Z Creme Brulee Cashews Recalled for Undeclared Walnut
Pilgrim's Roasted Nut'Z Creme Brulee Cashews are recalled for undeclared walnut. The product was distributed in California, Oregon, and Washington and poses a risk to consumers with walnut allergies.
Product
Pilgrim's Roasted Nut'Z Creme Brulee Cashews are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares Cashews, Sugar, French Vanilla Syrup, Caramel Syrup.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1161-2023·2023-03-01
Sterile Oncology Port Access Tray Recalled for Sterilization Failure
Medline is recalling sterile oncology port access trays in which some components were not properly sterilized due to improper placement during manufacturing. Healthcare facilities should immediately discontinue use of affected units.
Product
Medline Sterile Oncology Port Access Tray, Item #DYNDC2239, 20 sterile kits per case, containing Ethicon Biopatch Protective Disk with CHG, Disk with Chlorhexidine Gluconate (CHG), DRSG Biopatch 1IN NS, VPN: 10150;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0347-2023·2023-03-01
Sodium Chloride Injection Recalled for Incomplete Seal and Potential Leakage
B. Braun Medical is recalling 0.9% Sodium Chloride Injection due to possible incomplete container seals that may leak. The recall involves 483,229 bags distributed nationwide.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V131000·2023-02-28
2023 Nissan Ariya recalled for potentially loose steering wheel bolts
Nissan North America is recalling 2023 Ariya vehicles with potentially loose or missing steering wheel bolts. A detached steering wheel could cause loss of steering control and increase crash risk.
Product
NISSAN — 2023 NISSAN ARIYA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V129000·2023-02-27
Royal Enfield Himalayan motorcycles recalled for brake caliper corrosion
Royal Enfield is recalling 2017-2021 Himalayan motorcycles because road salt may corrode brake calipers, potentially causing brake failure and increasing crash risk.
Product
ROYAL ENFIELD — 2021 ROYAL ENFIELD HIMALAYAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V128000·2023-02-24
2023 Ford Expedition front axle may fracture, increasing crash risk
Ford is recalling certain 2023 Expeditions, along with F-150 and Lincoln Navigator vehicles, due to a front axle pinion defect that may not have been properly heat-treated. The defect can cause fracture, loss of 4-wheel drive, and wheel lockup, increasing crash risk.
Product
FORD — 2023 FORD EXPEDITION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V121000·2023-02-24
Thor Motor Coach recreational vehicles recalled for detaching overhead cabinets
Thor Motor Coach is recalling 2018-2021 Windsport and Hurricane recreational vehicles because the driver and front passenger overhead cabinets may detach while in motion, risking injury to occupants.
Product
THOR MOTOR COACH — 2021 THOR MOTOR COACH WINDSPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V123000·2023-02-24
2023 BMW S 1000 RR Motorcycles Recalled for Hand Brake Defect
BMW of North America is recalling certain 2023 S 1000 RR motorcycles due to a hand brake lever defect that may reduce brake performance. Approximately 394 units are affected.
Product
BMW — 2023 BMW S 1000 RR
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·23136·2023-02-23
LumaRail Bed Assist Rails recalled for entrapment and asphyxia hazard
Platinum Health is recalling about 53,000 LumaRail bed assist rails because users can become entrapped between the rail and mattress, risking death by asphyxiation. One death has been reported.
Product
LumaRail Bed Assist Rails
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·23V120000·2023-02-23
2022–2024 International and IC Bus Trucks/Buses: Engine Control Software Defect
Navistar is recalling 2022-2024 International HV and MV trucks and 2022-2023 IC Bus TC buses. An engine control module software defect can cause the engine to override the parking brake when the transmission remains in drive or reverse and the power take-off switch is engaged, resulting in unintended vehicle movement.
Product
INTERNATIONAL — 2022 INTERNATIONAL HV
Category
Vehicle
Distribution
Distributed nationwide

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