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

23201–23225 of 90098

SevereFDA (Devices)·Z-1763-2022·2022-10-05
TANDEM LIFE controller software failures affecting cardiopulmonary bypass equipment nationwide
FDA recalls TANDEM LIFE LivaNova LIFESPARC Controllers due to critical software failures that cause the device to freeze, crash, or stop displaying data. The controllers are used in cardiopulmonary bypass procedures.
Product
TANDEM LIFE LivaNova LIFESPARC Controller; Controller and Accessories Model 5900-0000; Controller Only Model 5900-0001. For circulatory or cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1791-2022·2022-10-05
Chocolate to Die For Premium Ice Cream recalled for undeclared peanuts
Belfonte Ice Cream's Chocolate to Die For Premium Ice Cream may contain undeclared peanuts. Affected products were sold at Hy-Vee, Cash Saver, Harps, Price Mart, and Heartland in Kansas City, Tulsa, Columbia, and Springfield areas.
Product
1.5 quarts (1.41 L) Chocolate to Die For Premium Ice Cream UPC: 83057 17049 Plant Code 29-050
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1798-2022·2022-10-05
Aged Raw Milk Cheese Recalled for Listeria Contamination Risk
Keswick Creamery recalls Calverley aged raw milk cheese due to potential Listeria monocytogenes contamination affecting products distributed to farm stores and farmers markets in DC, MD, VA, and PA.
Product
Aged raw milk cheese "Calverley" 4 oz to 12 oz packages
Category
Food
Distribution
5 states
SevereFDA (Food)·F-1801-2022·2022-10-05
Pasteurized Havarti cheese recalled for potential Listeria contamination
Keswick Creamery is recalling Havarti cheese due to potential Listeria monocytogenes contamination. All products manufactured by the firm may be affected.
Product
Pasteurized milk cheese "Havarti" 4 oz to 12 oz packages
Category
Food
Distribution
5 states
SevereFDA (Food)·F-1799-2022·2022-10-05
Aged Raw Milk Feta Cheese Recalled for Listeria Risk
Keswick Creamery is recalling aged raw milk feta cheese due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in DC, Maryland, Virginia, and Pennsylvania.
Product
Aged raw milk cheese "Feta" in 4 oz to 12 oz packages
Category
Food
Distribution
5 states
SevereNHTSA·22V740000·2022-10-05
Blue Bird Recalls 2022-2023 Vision Transit Buses Due to Fuel Leak Risk
Blue Bird is recalling 2022-2023 Vision transit buses with 7.3L gasoline engines because a transmission cable may cause a fuel leak, increasing fire risk.
Product
BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1795-2022·2022-10-05
Aged raw milk cheese recalled for potential Listeria monocytogenes contamination
Keswick Creamery is recalling Ploughman Cider Wash Tomme aged raw milk cheese (batch 47) due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in Washington DC, MD, VA, and PA.
Product
Aged raw milk cheese "Ploughman Cider Wash Tomme" batch 47 4 oz to 12 oz packages
Category
Food
Distribution
5 states
SevereFDA (Food)·F-1804-2022·2022-10-05
Vermeer Cheese Products Recalled for Potential Listeria Contamination
Keswick Creamery is recalling Vermeer Cheese due to potential Listeria monocytogenes contamination. Products were distributed to farm stores and farmers markets in Washington DC, Maryland, Virginia, and Pennsylvania.
Product
Vermeer Cheese in 4 oz to 12 oz packages
Category
Food
Distribution
5 states
SevereFDA (Food)·F-1793-2022·2022-10-05
Yellow Squash from Southeast Processing Recalled for Listeria monocytogenes
Southeast Processing Ltd is recalling yellow squash sold in multiple forms due to positive detection of Listeria monocytogenes in product samples. The affected product was distributed to Georgia and South Carolina.
Product
Yellow Squash sold as Bulk, Diced, Half Moon Sliced, Julienne and Planks (Product codes 168-173)
Category
Food
Distribution
2 states
HighFDA (Food)·F-1805-2022·2022-10-05
Alexia Organic Seasoned Hashed Browns recalled for potential Listeria contamination
Lamb Weston Sales is recalling Alexia Organic Seasoned Hashed Browns Yukon Select Potatoes due to potential Listeria monocytogenes contamination. The frozen product was distributed nationwide and internationally.
Product
Item AX058, Alexia Organic Seasoned Hashed Browns Yukon Select Potatoes, 16 oz. bag, 12/16 oz. bags per case. Product is frozen and it's not ready to eat and labeled with cooking instructions. Produced by Lamb Weston, Kennewick, WA. UPC 8 34183 00303 5. Product contains…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1790-2022·2022-10-05
Alida's Samoon Pita Bread recalled for undeclared soy allergen
Alida's Bakery is recalling Alida's Samoon Pita Bread because canola oil used in production contained undeclared soy lecithin. The recall affects 19 bags distributed in Washington state.
Product
Alida's Samoon Pita Bread, 4 pieces per package, net wt. 21 oz. UPC 8 60004 65933 4. Product contains ingredients: While Flour, Water, Wheat Gluten, Yeast, Sorbitan monostearate, ascorbic acid, Salt, Canola Oil. CONTAINS: Wheat, Gluten.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1855-2022·2022-10-05
Medline ClearPro Suction Catheter Connector May Separate During Use
Medline ClearPro closed suction catheters may have a connector that separates from the device during patient suctioning. The malfunction affects 65,320 units distributed nationwide and internationally.
Product
MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. ET LENGTH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12; b. ET LENGTH DOUBLE SWIVEL, 14 Fr, Item…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1830-2022·2022-10-05
Cope Mandril Wire Guide Guidewires Recalled for Packaging Seal Breach
Cook Incorporated is recalling Cope Mandril Wire Guide stainless steel guidewires because the packaging chevron seal may be completely breached, compromising device sterility. Affected lots total 2,748 units in the US and 302 internationally.
Product
Cope Mandril Wire Guide (Stainless Steel), Stainless Steel Guidewire Reference Part Number/GPN PMG-18SP-60-COPE G05183 PMG-18SP-100-COPE G05822 PMG-18SP-125-COPE G10077
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1839-2022·2022-10-05
Cook Roadrunner Guidewire Recalled for Compromised Sterile Packaging Seal
Cook Incorporated is recalling Roadrunner PC Wire Guide guidewires due to a complete breach of the sterile packaging seal. The breach may compromise device sterility, affecting 202 units in the US and 11 internationally.
Product
Roadrunner PC Wire Guide (Nimble Floppy), Guidewire RFPC-35-145 G07914
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1794-2022·2022-10-05
Organic GreenWise Animal Crackers recalled for undeclared tree nut allergen
Toufayan Bakery is recalling Organic GreenWise Animal Crackers due to undeclared coconut (tree nut) on the label. Consumers with tree nut allergies should not consume this product.
Product
Organic GreenWise Animal Crackers, NET WT 8 OZ (227 g)
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1840-2022·2022-10-05
Cook Roadrunner PC Guidewire Recalled for Compromised Packaging Seal
Cook Incorporated recalls Roadrunner PC Wire Guide devices due to a potential packaging seal breach that may compromise sterility. The recall affects 115 units distributed domestically and internationally.
Product
Roadrunner PC Wire Guide (The Firm LT), Guidewire Reference Part Number/GPN RLPC-35-145 G06866
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V741000·2022-10-05
2023 BMW iX Transmission Defect Risk of Vehicle Rollaway
BMW is recalling one 2023 iX with a defective transmission final drive gear weld that could break, causing vehicle rollaway if the parking brake is not engaged. Dealers will replace the electric drive unit at no cost.
Product
BMW — BMW IX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1826-2022·2022-10-05
Bentson Wire Guide Devices Recalled for Potential Sterility Compromise
Cook Incorporated is recalling Bentson Wire Guide devices due to potential packaging defects that may compromise device sterility.
Product
Bentson Wire Guide, Guidewire (OUS ONLY); Reference Part Number: TSMB-35-145 (GPN G27041)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1831-2022·2022-10-05
Cook Medical Wire Guide Devices Recalled for Packaging Breach
Cook Incorporated is recalling specific lots of Double Flexible Tipped Wire Guide Guidewire devices due to a complete breach of the packaging chevron seal, which may compromise sterility.
Product
Double Flexible Tipped Wire Guide, Guidewire Reference Part Number/GPN TDOC-35-145-0-3 G00362 C-TDOC-18-50-0-2 G05146 TDOC-35-50-0-3 G00364 C-DOC-21-40-0-2 G02431 C-TDOC-21-50-0-2 G05195 C-TDOC-25-50-0-2 G05145
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1812-2022·2022-10-05
t:slim X2 Insulin Pumps Recalled for Software Issues Affecting Blood Sugar Management
Tandem Diabetes Care is recalling approximately 8,399 t:slim X2 insulin pumps due to software malfunctions that may affect blood sugar control. A software update is available to resolve the issues.
Product
t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim x2 insulin pump with the Control-IQ Technology
Category
Medical Device
Distribution
53 states
HighFDA (Food)·F-1788-2022·2022-10-05
Alida's Saoka Pita Bread recalled for undeclared soy allergen
Alida's Saoka Pita Bread contains undeclared soy lecithin from cooking oil, posing a risk to people with soy allergies. The product was distributed in Washington state.
Product
Alida's Saoka Pita Bread, 5 pieces per package. Net Wt. 16.25 oz. UPC 8 60004 65930 3. Product contains ingredients: White Flour, Water, Wheat Gluten, Yeast, Sorbitan monostearate, ascorbic acid, Salt, Canola Oil. CONTAINS: Wheat, Gluten.
Category
Food
Distribution
1 state
HighFDA (Food)·F-1792-2022·2022-10-05
A&W Root Beer Zero Sugar Recalled for Undeclared Sugar Content
A&W Root Beer Zero Sugar in 20oz bottles is being recalled because it contains full sugar but is labeled as sugar-free. The affected product has lot number 071892 and was distributed in DC, MD, PA, and VA.
Product
"A&W Root Beer Zero Sugar" packaged in 20oz PET bottles. UPC: 00-0-78000-05340-1
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-1785-2022·2022-10-05
BD Pyxis MedBank Cabinet Software Update Prevents Drawer Access
A software update for BD Pyxis MedBank medication dispensing cabinets contains an incompatible file that prevents Matrix drawers from opening, potentially delaying medication access in healthcare facilities.
Product
BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 . MedBank 200 Main operating with Windows 7 . MedBank 500 Main operating with Windows 7. An automated dispensing cabinet…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2022·2022-10-05
Barco Medical Network Adapter Recalled for Installation Issues
Barco NV recalls 169 NexxisOR system network adapters (models K9303078A and K9303097A) due to installation issues. The affected devices were distributed in Florida, Illinois, and New Jersey.
Product
Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1837-2022·2022-10-05
Cook Roadrunner PC Guidewires Recalled for Compromised Packaging Sterility
Cook Incorporated is recalling Roadrunner PC Hydrophilic Guidewires due to potential packaging seal breaches that may compromise device sterility. Affected devices were distributed in the United States and internationally.
Product
Roadrunner PC Hydrophilic Wire Guide, Hydrophilic Guidewire Reference Part Number/GPN: RPC-035145-0-5 G34131 RPC-035145 G18154 RPC-035145-5 G34132 RPC-038145-0-5 G34129 RFSPC-038145-0 G17539 RFSPC-035145 G17540 RPC-038145-0 G18155 RPC-035145-0 G18153 RFSPC-035145-0…
Category
Medical Device
Distribution
Distributed nationwide

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23201–23225 of 90098