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

16001–16025 of 27769

HighFDA (Drugs)·D-0017-2024·2023-10-11
Fentanyl and Bupivacaine Injectable Bags Recalled for Sterility Assurance Issues
Central Admixture Pharmacy Services Inc. is recalling fentanyl-bupivacaine injectable solution due to lack of sterility assurance. The recall affects 190 units (250 mL bags) distributed nationwide.
Product
fentaNYL 2 mcg/mL and bupivacaine 0.125% PF in 0.9% sodium chloride / Total Volume = 250 mL, Total fentaNYL 500 mcg/250 mL, bag, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2082-2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0013-2024·2023-10-11
Guider Softip Guide Catheter with Incorrect Tip Curve Shape
Boston Scientific is recalling Guider Softip Guide Catheters due to an incorrect tip curve shape that differs from the labeled specification. The affected units may not perform as intended during cardiac procedures.
Product
Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE, Catalog number H965100470, cardiac guide catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2656-2023·2023-10-11
GE F2-01 Frame Patient Monitor Communication Interruption Risk
GE F2-01 Frame physiological patient monitors may experience data communication interruptions with CARESCAPE ONE and CARESCAPE Canvas 1000 monitors if not powered down within 120 days.
Product
F2-01 Frame, physiological patient monitor (with arrhythmia detection or alarms)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2662-2023·2023-10-11
Veran Endobronchial Navigation Devices Recalled for Design Non-Conformance and EMC Issues
Olympus Corporation recalls Veran endobronchial navigation devices due to manufacturing non-conformances and insufficient electromagnetic compatibility. Approximately 6,318 units distributed worldwide are affected.
Product
Veran : Endobronchial Models: INS-5500 View Optical Probe INS-5450 SPiN Xtend¿ 21ga, 1.8 OD, 5/Bx INS-5440 View Peripheral Catheter, 3.8mm OD, 2.5mm WC INS-5411 0.016" Stylet, 1235 mm L, 10/Bx INS-5410 SPiN Flex¿ ANSO¿ Needle, 22ga, 1.8mm OD, 5/Bx
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0011-2024·2023-10-11
Fentanyl Injection Recalled Due to Lack of Sterility Assurance
Central Admixture Pharmacy Services Inc. is recalling 688 units of fentanyl injection nationwide because it cannot assure the product meets sterility standards.
Product
fentaNYL in 0.9% sodium chloride, 500 mcg/50 mL, (10 mcg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2071-3
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0005-2024·2023-10-11
Phenylephrine injectable drug recalled due to sterility assurance failure
Central Admixture Pharmacy Services Inc is recalling 3,384 phenylephrine syringes due to lack of assurance of sterility. The product was distributed nationwide.
Product
PHENYLephrine in 0.9 sodium chloride, 400 mcg/10 mL, (40 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6007-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0031-2024·2023-10-11
FDA Recalls Hydromorphone Syringes Over Sterility Assurance Issue
Central Admixture Pharmacy Services Inc is recalling 2,664 syringes of HYDROmorphone injectable solution (30 mg/30 mL) distributed nationwide. The recall was initiated due to lack of assurance of sterility.
Product
HYDROmorphone in 0.9% Sodium Chloride, 30 mg/30 mL, (1 mg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2012-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0008-2024·2023-10-11
VITROS Proboscis/Piston Assembly Recall for Assay Accuracy Defect
Ortho-Clinical Diagnostics is recalling 9,860 Proboscis/Piston Assemblies for VITROS diagnostic systems manufactured April-December 2022 due to a manufacturing defect that may cause falsely elevated drug assay results and delayed patient test results.
Product
Proboscis/Piston Assembly, Part Number J55375, for VITROS 5,1 FS Chemistry System (Product Code 6801375), VITROS 5,1 Chemistry System (Refurbished) (Product Code 6801890), VITROS 3600 Immunodiagnostic System (Product Code 6802783), VITROS 3600 Immunodiagnostic System (Refurbished
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0015-2024·2023-10-11
Fentanyl and Bupivacaine Injectable Syringes Recalled for Sterility Defect
Central Admixture Pharmacy Services Inc. is recalling 895 syringes of fentanyl and bupivacaine injectable solution due to lack of assurance of sterility. The recall affects all doses nationwide.
Product
fentaNYL 1.5 mcg/mL and bupivacaine 0.125% PF in 0.9% sodium chloride / Total Volume = 50 mL, Total fentaNYL 75 mcg/50 mL, 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2080-2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0038-2024·2023-10-11
AB Sciex 4500MD Triple Quad Mass Spectrometer Recall Due to Fire Risk
AB Sciex has recalled 38 units of the 4500MD Triple Quad Mass Spectrometer nationwide due to a rare risk of flame and electrode ejection from solvent leaks combined with electrical discharge.
Product
4500MD Triple Quad Mass Spectrometer, Part Number 5032522
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0002-2024·2023-10-11
JLM Roasted Salted Pecan Halves Recalled Due to Hazelnut Substitution
Lipari Foods is recalling JLM Roasted Salted Pecan Halves because the product contains hazelnuts instead of pecans, presenting a risk to consumers with tree nut allergies.
Product
JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale case. Lipari number 368729, UPC 094776110049
Category
Food
Distribution
8 states
SevereNHTSA·22V799000·2023-10-10
CAN-AM Ryker Motorcycles Recalled for Loose Harnesses Causing Engine Stall
CAN-AM is recalling 2019-2023 Ryker motorcycles because electrical harnesses in the front fenders may loosen and rub on the tire, causing a short circuit that can stall the engine while driving.
Product
CAN-AM — 2021 CAN-AM RYKER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V712000·2023-10-09
2022 Subaru Outback Windshield Defect May Cause Detachment in Crash
Subaru is recalling 42 2022 Outback and Impreza vehicles due to incorrect paint clearcoat that may insufficiently bond the windshield. The windshield could detach during a crash, increasing injury risk.
Product
SUBARU — 2022 SUBARU OUTBACK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V709000·2023-10-09
2020-2021 GMC Acadia rearview camera may fail due to improper connector crimping
General Motors is recalling certain 2020-2021 GMC Acadia vehicles with defective rearview camera coaxial cables that may fail or malfunction. The improperly crimped connectors can reduce rear visibility and increase crash risk.
Product
GMC — 2020 GMC ACADIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V710000·2023-10-09
2023 Cadillac LYRIQ Instrument Panel Software Error May Cause Display to Go Blank
General Motors is recalling certain 2023 Cadillac LYRIQ vehicles due to a software error that may cause the instrument panel display to go blank, potentially preventing drivers from seeing critical safety information.
Product
CADILLAC — 2023 CADILLAC LYRIQ
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V708000·2023-10-09
2023 Cadillac XT6, XT5, and GMC Acadia: illegible tire certification label
General Motors is recalling 2023 Cadillac XT6, XT5, and GMC Acadia vehicles due to illegible tire size information on the driver's side certification label. The illegibility may result in incorrect tires being installed, increasing crash risk.
Product
CADILLAC — 2023 CADILLAC XT6
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V565000·2023-10-08
2023 Jeep Wrangler Brake Light Obstruction Recall
Chrysler is recalling certain 2023 Jeep Wrangler vehicles because the spare tire may obstruct the center high-mount brake light, reducing visibility to other drivers and increasing crash risk.
Product
JEEP — 2023 JEEP WRANGLER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V566000·2023-10-08
2022-2023 Toyota Tundra Fuel Tube Chafing Damage Recall
Toyota is recalling 2022-2023 Tundra and Tundra Hybrid vehicles because the plastic fuel tube may chafe against brake lines and leak fuel, creating a fire risk.
Product
TOYOTA — 2022 TOYOTA TUNDRA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V567000·2023-10-08
2022-2023 Chevrolet Bolt EV air bag deployment defect recall
General Motors is recalling certain 2022-2023 Chevrolet Bolt EV vehicles because the instrument panel cover may lack a required perforation, preventing proper passenger-side air bag deployment.
Product
CHEVROLET — 2022 CHEVROLET BOLT EV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V528000·2023-10-07
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·22V531000·2023-10-07
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·23V471000·2023-10-07
2023 BMW XM and 2024 X5-X7 vehicles recalled for knee air bag defect
BMW of North America is recalling 2023 XM and certain 2024 X5, X6, and X7 vehicles because the knee air bag may not have been manufactured correctly and could fail to deploy during a crash. Dealers will replace the air bag free of charge.
Product
BMW — 2023 BMW XM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V533000·2023-10-07
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
HighNHTSA·22V443000·2023-10-06
2022 Freightliner Cascadia brake system may fail to engage
The emergency braking system on certain 2022 Freightliner Cascadia trucks may fail to engage, creating a risk of brake failure. Dealers will install a corrective valve at no cost.
Product
FREIGHTLINER — 2022 FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V442000·2023-10-06
2022 Grand Design Momentum Travel Trailer Electrical Fire Hazard Recall
Grand Design is recalling 165 model-year 2022 Momentum travel trailers due to improper 110-volt electrical wiring that can overheat and create a fire risk. Dealers will rewire the power supply at no cost.
Product
GRAND DESIGN — 2022 GRAND DESIGN MOMENTUM
Category
Vehicle
Distribution
Distributed nationwide

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