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

19251–19275 of 27466

HighFDA (Devices)·Z-1153-2023·2023-03-01
ADVIA Centaur Folate 500 test kits recalled for inaccurate measurement results
Siemens Healthcare Diagnostics is recalling 7,884 ADVIA Centaur Folate 500 diagnostic test kits because using whole blood calibration with serum samples produces negative bias and inaccurate results.
Product
ADVIA Centaur Folate 500 test kit- For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10325366
Category
Medical Device
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 (Food)·F-0362-2023·2023-03-01
Pilgrim's Roasted Nut'Z Hazelnuts Recalled for Undeclared Milk
Pilgrim's Roasted Nut'Z Garlic, Parmesan, Cracked Black Pepper Hazelnuts are recalled due to undeclared milk, a major allergen.
Product
Pilgrim's Roasted Nut'Z Garlic, Parmesan, Cracked Black Pepper Hazelnuts are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares Hazelnuts, Sugar, Rehydrated Garlic, Cracked Black Pepper, Parmesan Cheese.
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 (Devices)·Z-1164-2023·2023-03-01
Luminos Agile Diagnostic Imaging System Collision Risk Recall
Siemens recalls Luminos Agile imaging systems that may collide with ceilings or walls due to default configuration settings, potentially causing serious injury to staff or patients.
Product
Luminos Agile with software VC10 - A diagnostic imaging system for radiographic and fluoroscopic studies. Model Number: 10502200
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
HighFDA (Drugs)·D-0336-2023·2023-03-01
Levothyroxine Oral Solution TIROSINT Recalled Due to Subpotency
IBSA PHARMA is recalling TIROSINT (levothyroxine sodium) oral solution due to subpotency in specific batches. The affected product may contain less active ingredient than labeled.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0340-2023·2023-03-01
FDA Recalls TIROSINT Levothyroxine Sodium Lot 220853 for Subpotency
IBSA Pharma Inc. recalled TIROSINT levothyroxine sodium lot 220853 nationwide due to subpotency. The oral solution may contain less active ingredient than labeled, potentially affecting thyroid hormone replacement therapy.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
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-0346-2023·2023-03-01
FDA Recalls Sodium Chloride Injection Due to Incomplete Container Seals
B. Braun Medical's 0.9% Sodium Chloride Injection batches recalled due to risk of incomplete seals that could allow leakage, potentially compromising sterility. The recall affects 1,343,982 bags distributed nationwide.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
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-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 (Devices)·Z-1167-2023·2023-03-01
Diagnostic imaging system recalled for collision risk from default settings
Siemens Luminos dRF Max diagnostic imaging systems are being recalled due to a risk of collision with ceiling, walls, or nearby objects caused by default room configuration settings. This could result in serious injury to staff or patients.
Product
Luminos dRF Max with software VE10, VF10, VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762471
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0404-2023·2023-03-01
Cajun Seasoning recalled for elevated aflatoxin levels
Tampico Spice Company is recalling Cajun Seasoning in multiple sizes due to elevated aflatoxin contamination. Affected lots were distributed across eight states.
Product
Cajun Seasoning 1 OZ, 1 LB, 1.5 LBS, 2 LBS, 5 LBS, 6 LBS units
Category
Food
Distribution
8 states
HighFDA (Food)·F-0358-2023·2023-03-01
Gordon Choice Cranberry Orange Nut Muffin Batter Recalled for Undeclared Soy
BAKE'N JOY FOODS is recalling Gordon Choice Cranberry Orange Flavored Nut muffin batter due to undeclared soy lecithin. Consumers with soy allergies face a reaction risk.
Product
Gordon Choice Cranberry Orange Flavored Nut muffin batter; 8lbs; packaged in pails
Category
Food
Distribution
1 state
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-1157-2023·2023-03-01
IV START KIT Connector Defect May Cause Fluid Leaks
Cardinal Health's Presource Packs IV START KIT is being recalled due to a manufacturing defect in the connector that may cause fluid leaks and compromise intravenous fluid delivery.
Product
Cardinal Health Presource Packs IV START KIT- Intended for IV access device CATALOG #: 01-5798B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1154-2023·2023-03-01
Folate test kits recalled for calibration error causing inaccurate results
Siemens is recalling ADVIA Centaur Folate 500 test kits because a calibration error causes inaccurate, falsely low results when testing serum samples, potentially affecting diagnostic accuracy.
Product
ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10331250 Siemens Material Number (SMN): 10325366
Category
Medical Device
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 (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
HighFDA (Drugs)·D-0330-2023·2023-03-01
Tacrolimus Capsules Recalled for Wrong-Strength Tablets Co-Mingled in Bottles
Dr. Reddy's Laboratories is recalling Tacrolimus 0.5 mg capsules due to the presence of one 1 mg capsule co-mingled in affected bottles. The mismatched capsule could lead to incorrect dosing in immunosuppressed patients.
Product
TACROLIMUS — TACROLIMUS (TACROLIMUS)
Category
Drug
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 (Food)·F-0385-2023·2023-03-01
Cashew Crave Mix recalled due to undeclared milk and soy allergens
Nature's Eats Cashew Crave Mix 8 oz. is recalled for undeclared milk and soy allergens. The allergens are present in the product but not declared in the main 'Contains' statement.
Product
Nature's Eats Cashew Crave Mix 8 oz. UPC 8-10087-30330-3, packaged in cello bags 12 packages per case
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-1162-2023·2023-03-01
Medline Sterile Maximum Barrier Pack-LF units recalled for sterilization failure
Medline Industries recalls approximately 720 Sterile Maximum Barrier Pack-LF units due to improper component placement preventing sterilization. The affected packs were distributed in Arkansas, Colorado, and Georgia.
Product
(1) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546C, 6 kits per case, contains BD Chloraprep Hi-Lite Orange, 10.5 mL Applicator, Vendor PN: 930715NS; (2) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546D, 6 kits per case, contains BD Chloraprep Hi-Lite Oran
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0364-2023·2023-03-01
Pilgrim's Roasted Nut'Z Chocolate Espresso Beans recalled for undeclared soy
Pilgrim's Roasted Nut'Z Tri-Colored Chocolate Espresso Beans are recalled due to undeclared soy lecithin. Consumers with soy allergies may experience allergic reactions.
Product
Pilgrim's Roasted Nut'Z Tri-Colored Chocolate Espresso Beans are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares Espresso Beans, Dark Chocolate, Milk Chocolate, Marbled White Chocolate.
Category
Food
Distribution
0 states

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