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

22826–22850 of 26059

HighFDA (Food)·F-0628-2022·2022-02-09
Delizza Belgian Mini Cream Puffs Recalled Due to Metal Contamination
Poppies International is recalling Delizza Belgian Mini Cream Puffs due to metal fragments found in the palm oil silo. The metal was not consistently detected during production screening.
Product
Delizza BELGIAN MINI CREAM PUFFS WHIPPED FILLING MADE WITH FRESH CREAM NET WT 13.2 oz (375g) PRODUCED IN THE US BY DELIZZA INCORPORATED 6610 CORPORATION PARKWAY, BATTLEBORO, NC 27809 UPC: 6 76670 00107 6, and NET WT. 3lb 5 oz. (1.5kg) 120ct UPC: 6 76670 00800 6
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-0537-2022·2022-02-09
DIXI Medical Microdeep Depth Electrode Packaging Defect Threatens Sterile Barrier
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes due to potential packaging deformation that could compromise the sterile barrier. Approximately 2,720 units were distributed nationwide for use in brain recording and stimulation procedures.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length va
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V069000·2022-02-09
Seat belt pretensioners may explode in recalled 2021 Hyundai Accent vehicles
Hyundai recalls 2021 Accent vehicles due to defective seat belt pretensioners that may explode in a crash and project metal fragments, risking injury to occupants.
Product
HYUNDAI — 2021 HYUNDAI ACCENT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0555-2022·2022-02-09
Young Dental Sterilization Indicator Labels May Contain Wrong Type
YOUNG DH Dry Heat Indicator Labels used in healthcare sterilization may contain TTS Indicator Labels instead. Healthcare providers should verify package contents before use to ensure proper sterilization monitoring.
Product
YOUNG DH Dry Heat Indicators, PRESSURE SENSITIVE LABELS with COLOR INDICATOR STRIP, REF 116312 Intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor one or more parameters of the sterilization process
Category
Medical Device
Distribution
0 states
HighCPSC·22075·2022-02-09
Pittsburgh Automotive Pneumatic Roller Seats Recall Due to Fall Hazard
Harbor Freight Tools is recalling Pittsburgh Automotive pneumatic roller seats because the connection between the seat and post can break, causing users to fall. The company has received 96 reports of seat welds breaking, including 10 reports of minor injuries.
Product
Pittsburgh Automotive Pneumatic Roller Seats
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0627-2022·2022-02-09
Delizza Chocolate Cream Puffs Recalled for Metal Contamination
Delizza Belgian Mini Chocolate Cream Puffs are recalled due to small metal pieces found in the bakery's palm oil silo that could not be reliably detected by the manufacturer's metal detector system.
Product
Delizza BELGIAN MINI CHOCOLATE CREAM PUFFS NET WT. 14.1 oz (400g) 30 CREAM PUFFS PRODUCED IN THE US BY DELIZZA INCORPORATED 6610 CORPORATION PARKWAY, BATTLEBORO, NC 27809 UPC 6 76670 00402 2
Category
Food
Distribution
4 states
HighFDA (Food)·F-0624-2022·2022-02-09
Walla Walla Cheese Cheddar Curds recalled due to under-pasteurization
Walla Walla Cheese Company is recalling Cheddar Curds due to under-pasteurization of the milk used in production, which may not eliminate potentially harmful bacteria.
Product
Walla Walla Cheese Company Cheddar Curds. Keep Refrigerated. Product is packaged in vacuum sealed zip lock bags. Net wt. 5 lbs.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-0557-2022·2022-02-09
Chameleon PTA Balloon Catheter difficult protector sleeve removal risk
The Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm has a protector sleeve that may be difficult to remove, potentially damaging the balloon and causing patient harm. Covidien is recalling 1,994 devices.
Product
Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm, Chameleon PTA Balloon Catheter with Injection Port 8 mm x 40 mm; Cardiovascular. Product Numbers CH08-40-75GB and CH08-40-75US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2022·2022-02-09
Vagus Nerve Stimulation Therapy Leads Recalled for Tubing Wall Defect
LivaNova's PerenniaDURA vagus nerve stimulation leads may have insufficient silicone tubing thickness due to a manufacturing issue. This could result in unintended stimulation delivery or loss of therapy if the tubing is breached.
Product
Vagus Nerve Stimulation (VNS) Therapy Leads, PerenniaDURA, Model: 303. Model 303-20 PereniaDURA Lead (2.0 mm electrode inner diameter) and Model 303-30 PereniaDURA Lead (3.0 mm electrode inner diameter)
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0541-2022·2022-02-09
DIXI Microdeep Depth Electrodes recalled for potential packaging deformation compromising sterility
DIXI MEDICAL USA is recalling 1792 Microdeep Depth Electrodes due to potential deformation of the internal blister pack that could compromise the sterile barrier when the device is removed from its Tyvek bag.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length va
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V067000·2022-02-08
Holiday House Travel Trailers Propane Regulator Failure Risk
Holiday House is recalling certain 2019–2021 travel trailers equipped with defective Winntec propane regulators that may fail and increase propane pressure, raising fire risk in gas appliances.
Product
HOLIDAY HOUSE — 2019 HOLIDAY HOUSE 24TB
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V068000·2022-02-08
Tiffin motorhomes have improperly secured buss bars increasing fire risk
Tiffin is recalling 2018-2022 Allegro and Allegro Breeze motorhomes where an improperly secured electrical buss bar can cause the DC Distribution Panel to overheat and potentially start fires. Dealers will replace the buss bar with a cable for free.
Product
TIFFIN — 2018 TIFFIN ALLEGRO BREEZE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V065000·2022-02-07
Roadtrek Recreational Vehicles Recalled for Unattached Propane Lines
Roadtrek is recalling certain 2021-2022 recreational vehicles because the propane line may not be attached to the water heater. An unattached propane line can allow gas to enter the vehicle, increasing the risk of a fire.
Product
ROADTREK — 2021 ROADTREK PLAY SLUMBER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V063000·2022-02-04
Tesla Model Y Boombox Feature May Obscure Pedestrian Warning System
Tesla is recalling certain 2020-2022 Model Y vehicles because the Boombox feature can obscure the Pedestrian Warning System sounds, creating a collision risk. Tesla will disable the Boombox in Drive, Neutral, and Reverse modes via software update.
Product
TESLA — 2020 TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22719·2022-02-03
River Street Five-Drawer Chests Recalled for Tip-Over and Entrapment Hazards
BFG North Carolina is recalling about 1,380 River Street Five-Drawer Chests sold at Rooms To Go from February 2019 through October 2021. The dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that may result in death or serious injuries to children.
Product
River Street Five-Drawer Chests
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V059000·2022-02-03
Class C Motorhomes Recalled for Defective Steering Bolts
Jayco is recalling certain 2021-2022 Entegra Coach Accolade and Jayco Seneca Class C motorhomes because steering arm and tie rod bolts may fracture, causing loss of steering control. Free replacement available.
Product
ENTEGRA — 2021 ENTEGRA ACCOLADE XL
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0548-2022·2022-02-02
Fresh Express Salad Kits Recalled for Potential Listeria Contamination
Fresh Express Inc is recalling Chopped Kit Thai 'N' Cashews salad products due to potential contamination with Listeria monocytogenes. The recall affects 21,053 cases distributed across multiple U.S. states and Canada.
Product
"Chopped Kit Thai "N" Cashews" (salad product) packed in 11.7oz. packages
Category
Food
Distribution
20 states
CriticalFDA (Food)·F-0609-2022·2022-02-02
Twisted Chopped Caesar salad recalled for potential Listeria contamination
Fresh Express Inc is recalling Twisted Chopped Caesar salad in 9.4oz packages due to potential Listeria monocytogenes contamination. The product was distributed to retailers in 20 U.S. states and Canada.
Product
"Twisted Chopped Caesar" (salad product) packed in 9.4oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0538-2022·2022-02-02
Fresh Express Chicken Caesar Bowl Salad Recalled for Listeria Risk
Fresh Express Inc is recalling Chicken Caesar Bowl salads in 5.7oz and 5.75oz packages due to potential Listeria monocytogenes contamination. The product was distributed to domestic and Canadian distributors.
Product
"Chicken Caesar Bowl" (salad product) packed in 5.7oz. and 5.75oz. packages
Category
Food
Distribution
20 states
SevereFDA (Drugs)·D-0407-2022·2022-02-02
Mitomycin-C Injectable Syringes Recalled for Sterility Assurance Failure
Edge Pharma is recalling Mitomycin-C 40 mg/40 mL single-dose syringes (NDC 05446-1416-01) nationwide due to lack of assurance of sterility. Approximately 860 syringes are affected.
Product
Mitomycin-C, 40mg/40mL (1mg/mL), 40 mL per syringe, Single Dose Syringe for Intravesical Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1416-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0549-2022·2022-02-02
Fresh Express Chopped Pomegranate Salad Recalled for Listeria
Fresh Express Inc is recalling Chopped Pomegranate salad in 10.3 oz packages due to potential Listeria monocytogenes contamination. The product was distributed to retailers and distributors across 20 U.S. states and Canada.
Product
"Chopped Pomegranate" (salad product) packed in 10.3oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0563-2022·2022-02-02
Italian Salad Product Recalled for Listeria Contamination Risk
Fresh Express Inc is recalling Italian salad in 9oz. packages due to potential Listeria monocytogenes contamination. The affected product was distributed to retailers across the United States and Canada.
Product
"Italian" (salad product) packed in 9oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0527-2022·2022-02-02
Fresh Express Avocado Ranch Salad Recalled for Listeria Risk
Fresh Express Inc is recalling Avocado Ranch salad products in 9.7oz and 12.8oz packages due to potential Listeria monocytogenes contamination. The products were distributed to wholesalers across 20 U.S. states and Canada.
Product
"Avocado Ranch" (salad product) packed in 9.7oz. and 12.8oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0593-2022·2022-02-02
Romaine Garden Salad Recalled for Potential Listeria Contamination
Fresh Express Inc is recalling Romaine Garden salad in 12oz. packages due to potential contamination with Listeria monocytogenes. The product was distributed to domestic and Canadian distributors across multiple states.
Product
"Romaine Garden" (salad product) packed in 12oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0604-2022·2022-02-02
Sweet Dijon Onion Salad Recalled for Listeria Contamination Risk
Fresh Express Inc is recalling Sweet Dijon Onion salad products in 7.6oz. packages due to potential Listeria monocytogenes contamination. The product was distributed to retailers across 20 US states and Canada.
Product
"Sweet Dijon Onion" (salad product) packed in 7.6oz. packages
Category
Food
Distribution
20 states

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