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

21576–21600 of 27001

HighFDA (Food)·F-1442-2022·2022-07-27
Chuckanut Bay Key Lime Cheesecake Bites Recalled for Undeclared Soy
Chuckanut Bay Foods LLC recalls Key Lime Cheesecake Bites (Item 32012-56, Lot 2C168A2) because the label fails to declare soy lecithin, posing a risk to consumers with soy allergies.
Product
Item 32012-56, Chuckanut Bay Key Lime Cheesecake Bites (Dark Compound) BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. The label is read in parts: BUTTER OIL, ENRICHED FLOUR (wheat flour ***), CRYSTALLIZED LIME***, SALT, CAROB BEAN
Category
Food
Distribution
13 states
HighFDA (Food)·F-1460-2022·2022-07-27
Grandma's Fudge Classic Truffle Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Grandma's Fudge Classic Truffle due to undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The product may pose a risk to individuals with tree nut allergies.
Product
Grandma's Fudge Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11062 7. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], sunflower lecithin & pure vanilla) honey, butter (pasteurized cream, salt), crea
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1416-2022·2022-07-27
Hill-Rom Centrella Pro+ mattress reduced heat-moisture management performance
Affected Hill-Rom Centrella Pro+ 36-inch mattresses may have reduced Microclimate Management performance, increasing risk of pressure ulcer development. The failure affects heat and moisture control.
Product
Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1276-2022·2022-07-27
Nephron Phenylephrine HCl Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center LLC recalls Phenylephrine HCl Injection (1 mg/10 mL) syringes nationwide due to inability to guarantee sterility. Approximately 464,265 syringes across eleven lot numbers are affected.
Product
Phenylephrine HCl Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-957-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1429-2022·2022-07-27
Spinal fixation removal key fracture risk under misuse conditions
The ENNOVATE MIS removal key used in spinal fixation systems may fracture if the 90-degree angle is not maintained during use. A product redesign is underway.
Product
ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1391-2022·2022-07-27
Surgical knee implant instrument key may become nonfunctional during assembly
Aesculap is recalling the ENDURO SPECIAL KEY TIB.LOCK.RING (product code NP462R) used in knee replacement surgery because the key pins may be damaged during assembly, causing the instrument to become nonfunctional.
Product
ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during orthopedic implant surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1495-2022·2022-07-27
Truffle Gift Box Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Truffle Gift Boxes due to undeclared tree nuts that may pose a hazard to allergic consumers. Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Truffle Gift Box PLU Code: 788394 17655 5
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1449-2022·2022-07-27
Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Allergen
Chuckanut Bay Foods LLC is recalling Sharis Strawberry Cheesecake Bites (Lot Code 2C159A2) due to undeclared soy lecithin. The label lists sunflower lecithin when the product actually contains soy lecithin, posing a risk to consumers with soy allergies.
Product
Item 81109-12, Chuckanut Bay Sharis Strawberry Cheesecake Bites. Perishable - Keep Refrigerated. There are 9 pieces per pack and 12 packs per case. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CANE SUGAR, PASTEURIZED CULTURED MILK INGREDIENTS: CANE SUGAR, CR
Category
Food
Distribution
13 states
HighFDA (Food)·F-1496-2022·2022-07-27
Truffle Dark Gift Box Recalled for Undeclared Tree Nuts
Queen Bee Gardens recalls Truffle Dark Gift Box due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a risk to consumers with tree nut allergies.
Product
Truffle Dark Gift Box, 12 pc., 6 oz. PLU Code: 788394 17660 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1433-2022·2022-07-27
Revie Superfoods Heart Beet Smoothie Mix Recalled for Potential Norovirus
Revive Organics is recalling Revie Superfoods Heart Beet 206g Ready-to-Blend smoothie mix due to potential norovirus contamination in frozen raspberries used in the product. Consumers should not consume affected lots.
Product
Revie Superfoods Heart Beet 206g Ready-to-Blend Cardamom + Beet Smoothie Made in Canada UPC 8 53267 00112 5 Revive Superfoods 1880 Bonhill Road, Mississauga, Ontario, Canada
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1435-2022·2022-07-27
BD Connecta Stopcock Without Extension Tube Recalled for Potential Leakage Risk
Becton Dickinson & Company is recalling BD Connecta Stopcock units worldwide due to a potential housing leakage defect that could interrupt treatment or cause exposure to biohazardous material.
Product
BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1479-2022·2022-07-27
Honey Caramels Pecan Pearl Recalled for Undeclared Tree Nuts
Queen Bee Gardens recalls Honey Caramels Pecan Pearl due to potential undeclared tree nuts including almonds, coconut, macadamia, and walnuts that may pose a risk to consumers with allergies.
Product
Honey Caramels Pecan Pearl. Net wt. 5.87 oz. PLU Code: 788394 12804 2. Ingredients: Honey, butter (pasteurized cream & salt), cream, grade A fancy pecans, nonfat dry milk, whey, pure vanilla, lecithin, algin & agar.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1407-2022·2022-07-27
Nonsterile Components in Medical Convenience Kits Recalled
ROi CPS LLC is recalling 86 nonsterile medical convenience kits distributed in Missouri because components that were supposed to be sterile were packaged as nonsterile.
Product
Nonsterile convenience kits: (1) regard Item #830099008, CV01005H - CV Part 1 Bundle; and (2) regard Item #830019017, CV00214Q - CV.
Category
Medical Device
Distribution
1 state
HighFDA (Drugs)·D-1281-2022·2022-07-27
Succinylcholine Chloride Injection Recalled for Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling 18,840 syringes of Succinylcholine Chloride Injection nationwide because the manufacturing process cannot be assured to have maintained sterility.
Product
Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-919-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1498-2022·2022-07-27
Chocolate Sampler product recalled due to undeclared tree nuts
Queen Bee Gardens is recalling Chocolate Sampler 13 oz packages due to undeclared tree nuts. The products may contain pecans, almonds, coconut, macadamia nuts, or walnuts.
Product
Chocolate Sampler Net wt. 13 oz. PLU Code: 788394 76511 7
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1456-2022·2022-07-27
Chocolate Truffles Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Dark on Dark Classic Truffle products due to the potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts) that pose an allergen risk to sensitive consumers.
Product
Dark on Dark Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11030 6. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, non-fat dry milk, whey, agar, algin & lecithin.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1463-2022·2022-07-27
Truffle Recall: Undeclared Tree Nuts Present Allergen Risk
Queen Bee Gardens is recalling Midnight Gold Classic Truffles for potentially containing undeclared tree nuts, which pose a risk to allergic consumers. Distribution included Colorado, New Mexico, Wyoming, and nationwide online.
Product
Midnight Gold Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11070 2. Ingredients: Dark chocolate, honey, butter (pasteurized cream, salt), cream, non-fat dry milk, whey, almonds, milk chocolate, natural flavor, salt, soda, agar, algin & lecithin.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1448-2022·2022-07-27
Cervical spinal implant connectors may fail to maintain proper clamping force
Aesculap Implant Systems has recalled certain cervical spine implant connectors due to insufficient clamping force. The defect may allow movement on the rods or cause microparticle abrasion.
Product
AESCULAP S4 Cervical Cross Connector L 42-58mm, S4C CROSS CONNECTOR VARIABLE 42-58MM, product code SW117T. Used in spinal fusion surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1251-2022·2022-07-27
Epinephrine Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling 134,385 epinephrine injection syringes nationwide due to lack of assurance of sterility. No illnesses have been reported.
Product
EPINEPHrine Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-925-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1257-2022·2022-07-27
HYDROmorphone Injection Recalled Due to Lack of Sterility Assurance
HYDROmorphone HCl Injection 30 mg/30 mL from Nephron Sterile Compounding Center LLC is being recalled nationwide due to lack of assured sterility. The recall affects 18,570 syringes across three lot numbers.
Product
HYDROmorphone HCl Injection, USP 30 mg/30 mL (1 mg/mL) syringe, 5 x 30 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-559-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V528000·2022-07-22
2022 Ford F-53 Steering Wheel Attachment Bolt May Loosen
Ford is recalling certain 2022 F-53 and F-59 motorhome and commercial chassis vehicles because the steering wheel attachment bolt may loosen and separate. This could result in loss of steering control and increased crash risk.
Product
FORD — 2022 FORD F-53
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V531000·2022-07-22
Spartan RV Chassis Steering Gear Assembly Defect Recall
Shyft Group is recalling certain 2022-2023 Spartan RV Chassis vehicles due to improperly assembled steering gears that may fracture, causing loss of steering control. Owners should contact the manufacturer for free inspection and replacement.
Product
SPARTAN — 2023 SPARTAN K1
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V533000·2022-07-22
Mercedes-Benz AMG vehicles: transmission wiring fire hazard, 2019-2022
Mercedes-Benz has recalled certain 2019–2022 AMG vehicles (CLS53, E53, GT53, and GT43 models) due to transmission wiring harness misrouting that can expose electrical connectors to corrosion, creating a fire risk.
Product
MERCEDES-BENZ — 2021 MERCEDES-BENZ AMG CLS53
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V523000·2022-07-21
2022 and 2023 Land Rover Defender seat belt pretensioner defect recall
Jaguar Land Rover is recalling certain 2022-2023 Land Rover Defender and other models due to defective front seat belt pretensioners that may fail to properly restrain occupants in a crash, increasing injury risk.
Product
LAND ROVER — 2022 LAND ROVER DEFENDER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22759·2022-07-21
Monti Kids Toy Box with Bins Recalled Due to Choking Hazard
Monti Kids is recalling about 1,500 Toy Box with Bins units sold online from July 2021 through February 2022 because a small dowel can become exposed and detach, posing a choking hazard to young children.
Product
Monti Kids Toy Box with Bins
Category
Consumer Product
Distribution
Distributed nationwide

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21576–21600 of 27001