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

9851–9875 of 36631

SevereFDA (Devices)·Z-1284-2021·2021-03-31
Caire Diagnostics Recalls FenomPro Devices Due to Erroneous High FeNO Readings
Caire Diagnostics is recalling FenomPro devices because calibration drift and software errors may cause erroneously high FeNO readings, potentially leading to premature discontinuation of asthma treatment.
Product
CAIRE DIAGNOSTICS FenomPro REF 900-0001 SN ***** - Product Usage: a portable, non-invasive device to measure fractional exhaled nitric oxide (FeNO) in human breath. Fenom Pro should not be used in critical care, emergency care or in anesthesiology.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0312-2021·2021-03-31
Golden State Medical Supply Recalls Omeprazole Capsules Due to Impurities
Golden State Medical Supply is recalling Omeprazole Delayed Release Capsules because stability testing revealed unknown impurities.
Product
Omeprazole Delayed Release Capsules, USP, 20 mg, 1000-count bottles, Rx only, Packaged by GSMS Incorporated, Camarillo, CA 93012-8601 USA, NDC 51407-129-10
Category
Drug
Distribution
2 states
SevereFDA (Devices)·Z-1282-2021·2021-03-31
Hitachi Arietta 850 Ultrasound System Recalled for Acoustic Output Error
Hitachi Medical Systems America Inc. is recalling Arietta 850 ultrasound systems with specific software versions due to an error that can cause acoustic output to exceed regulatory limits.
Product
Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doctor, Sonographer, etc.) for the diagnostic ultrasound evaluation of Fetal, Abdominal, Intra-operative (Spec.), Intraoperative (Neuro.), Laparoscopic, Pediatric, Small Organ (Spec.)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0313-2021·2021-03-31
ICU Medical Recalls Sodium Chloride Irrigation Due to Particulate Matter
ICU Medical is recalling 425,628 bottles of 0.9% Sodium Chloride Irrigation due to the presence of particulate matter.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1307-2021·2021-03-31
Biomerieux Recalls VITEK 2 Systems Due to HL7 Software Defect
Biomerieux is recalling 8,786 VITEK 2 systems worldwide due to a software defect that may cause false susceptible results when using HL7 communication.
Product
VITEK 2 (version numbers 8.01, 8.02 (8.0x) and 9.01, 9.02 (9.0x) with the external communication configured to HL7 (system, test, automated, antimicrobial susceptibility, short incubation). VITEK 2 is an automated system consisting of instruments, software and reagent cards desi
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1280-2021·2021-03-31
Baxter Recalls Prismaflex Preventative Maintenance Kits Due to Tubing Performance Variability
Baxter Healthcare is recalling Prismaflex Preventative Maintenance Kits and spare part kits because tubing performance variability may cause alarms during or after system self-tests.
Product
Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and G5006203) - Product Usage: For Prismaflex Control Units, used for Continuous Renal Replacement Therapy (CRRT).
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V217000·2021-03-26
Mercedes-Benz Recalls AMG Models Due to Starter Cable Fire Risk
Mercedes-Benz is recalling 493 AMG E63S and GT63 models because an incorrectly installed starter cable may chafe wires, causing a short circuit, vehicle stall, or fire.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, AMG GT63, AMG GT63S
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V210000·2021-03-25
2021 Chevrolet Tahoe seat belt latch may be inaccessible
GM is recalling certain 2021 Chevrolet Tahoe vehicles because the second-row center seat belt latch may be trapped beneath the trim bezel. Passengers cannot use this seat belt, increasing injury risk in a crash.
Product
CHEVROLET — CHEVROLET TAHOE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V214000·2021-03-25
RV Chassis steering column defect may cause loss of steering
Shyft Group is recalling certain 2021-2022 Spartan RV Chassis K1-K4 vehicles. A steering column defect may cause the steering output shaft to disengage, resulting in loss of steering control and crash risk.
Product
SPARTAN — SPARTAN K3, K4, K2, K1
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·21732·2021-03-25
Polaris Recalls Ranger and Utility Vehicles Due to Fire Hazard
Polaris is recalling approximately 41,500 Ranger, ProXD, Gravely, and Bobcat off-road vehicles because a drive belt can break, damage the fuel line, and cause a fire.
Product
Model Year 2020-2021 RANGER 1000 and RANGER CREW 1000, Model Year 2020 ProXD 2000G and 4000G, Model Year 2020-2021 Ariens/Gravely JSV3200, JSV3400, and JSV6400, Model Year 2020 Bobcat UV34 4x4 GAS and UV34 XL GAS, and Model Year 2021 Bobcat UV34 4x4 GAS
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·21V215000·2021-03-25
Honda and Acura Recall Vehicles for Fuel Pump Failure Risk
Honda is recalling 2018-2020 Acura and Honda vehicles because the fuel pump may fail, causing the engine to stall while driving.
Product
ACURA — ACURA, HONDA TLX, RDX, CR-V, CIVIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V213000·2021-03-25
GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Steering Defect
General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon vehicles because a poor electrical connection may cause loss of power steering, increasing crash risk.
Product
CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0341-2021·2021-03-24
Kareem Mart Recalls Tahina Sesame Paste Due to Salmonella
Kareem Mart Inc is recalling Tahina Sesame Paste in 1lb, 2lb, and 10kg containers because the product tested positive for Salmonella.
Product
Tahina Sesame Paste packaged in 1lb and 2lb plastic jars and 10kg metal containers; UPC CODES 6215000382207
Category
Food
Distribution
8 states
CriticalFDA (Devices)·Z-1195-2021·2021-03-24
Medtronic Custom Perfusion Pack Recalled for Bacterial Endotoxin Levels
Medtronic is recalling 4 units of Custom Perfusion Packs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.
Product
Medtronic Custom Perfusion Pack (CUSTOM PACK HY11B40R1 1/4 RESPIRATO). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is collected, filte
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0342-2021·2021-03-24
Alqosh Sesame Oil Tahin Recalled Due to Salmonella Contamination
Mediterranean Food, Inc. is recalling Alqosh Sesame Oil Tahin in 2lb jars because the product tested positive for Salmonella.
Product
Alqosh Sesame Oil "Tahin" packaged in 2lb plastic jars
Category
Food
Distribution
1 state
SevereNHTSA·21V202000·2021-03-24
2020-2021 Ford F-53 and F-59 Motorhome Rear Bearing and Axle Defect
Ford is recalling certain 2020-2021 F-53 and F-59 motorhome and commercial chassis vehicles due to inadequate rear axle lubricant. The defect may cause rear wheel bearing damage, rear axle failure, and loss of motive power and brake function.
Product
FORD — FORD F-59, F-53
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V205000·2021-03-24
Tracker Recalls 2021 Trailers Due to Tire Fender Rubbing
Tracker Marine is recalling 2021 Ranger Trail and Trailstar trailers because tires may rub against fenders, causing premature wear and increasing the risk of a tire blowout.
Product
RANGER TRAIL — RANGER TRAIL, TRAILSTAR ZV20, NZ18, ZV21, NZ21
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V206000·2021-03-24
Western Star 4700 and 5700 Ground Harness Wiring Defect
DTNA is recalling 2019-2021 Western Star 4700 and 5700 vehicles with undersized ground harness wiring that may cause connector melting and engine stall, increasing crash risk. Owners should contact DTNA for free replacement.
Product
WESTERN STAR — WESTERN STAR 4700, 5700
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0305-2021·2021-03-24
Sagent Recalls Phenylephrine Hydrochloride Injection Due to Sterility Concerns
Sagent Pharmaceuticals is recalling specific lots of Phenylephrine Hydrochloride Injection due to customer complaints of loose vial overseals that may compromise sterility.
Product
PHENYLEPHRINE HYDROCHLORIDE — PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1196-2021·2021-03-24
Medtronic Affinity Pixie Cardiotomy Reservoir Recalled for Bacterial Endotoxin
Medtronic is recalling 70 units of Affinity Pixie Cardiotomy/Venous Reservoirs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.
Product
Custom Perfusion System (CUSTOM PACK BB10H89R4 ECLR). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is collected, filtered, and defoamed
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1262-2021·2021-03-24
Merit Medical Recalls HeartSpan Transseptal Needles Due to Tip Curvature Mismatch
Merit Medical Systems is recalling 587 HeartSpan Transseptal Needles because the labeled tip curvature may not match the actual curvature, posing a risk of unintended anatomy puncture.
Product
HeartSpan Transseptal Needles Catalog No. FND-019-01, Lot No. E1913644 consisting of an outer needle cannula and an inner stylet. The needle is comprised of flexible thin walled tubing with an ergonomic hub and stopcock attached to the proximal end. The stylet consists of a soli
Category
Medical Device
Distribution
18 states
SevereNHTSA·21V204000·2021-03-24
Jayco Recalls 2019-2020 Motorhomes Due to Gas Leak Risk
Jayco is recalling 2,144 motorhomes because a stove component may cause a gas leak, increasing the risk of fire.
Product
JAYCO — JAYCO, ENTEGRA GREYHAWK, ESTEEM, ODYSSEY, REDHAWK
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0339-2021·2021-03-24
Frozen Tuna Steaks Recalled Due to Salmonella Contamination
Seafood Imports Distributors Inc. is recalling 10 oz. frozen tuna steaks because FDA samples tested positive for Salmonella.
Product
Java Frozen Tuna Steaks - 10 oz. Net Wt. 10 lb. - Approximately 15-18 pieces individually vacuum packed. Product of Indonesia - Wild Caught.
Category
Food
Distribution
5 states
SevereNHTSA·21V200000·2021-03-24
Porsche Recalls 2021 Models Due to Engine Connecting Rod Defect
Porsche is recalling 2021 Cayman, Boxster, and 718 Spyder vehicles because engine connecting rods may crack and loosen, increasing the risk of a crash or fire.
Product
PORSCHE — PORSCHE redundant CAYMAN, redundant BOXSTER, 718 SPYDER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V203000·2021-03-24
Starcraft RV Recalls 2019-2020 Travel Trailers Due to Gas Leak Risk
Starcraft RV is recalling 2019-2020 travel trailers because an overtightened bolt may damage a seal, causing a gas leak that increases fire risk.
Product
STARCRAFT RV TT — STARCRAFT RV TT MOSSY OAK LITE, AUTUMN RIDGE, GPS, LAUNCH OUTFITTER
Category
Vehicle
Distribution
Distributed nationwide

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