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

9701–9725 of 31231

HighFDA (Devices)·Z-0657-2025·2024-12-25
Ambler Surgical Bipolar Pencil recalled for outer tube structural failure
Kirwan Surgical Products is recalling the Ambler Surgical Bipolar Pencil 25 Gauge Straight (Model PD7226) because the outer stainless-steel tube may break or detach during use. 4,470 units worldwide are affected.
Product
Ambler Surgical Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: PD7226. The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauterization of the retinal area durin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0310-2025·2024-12-25
Bakestone Brothers Pita Bread Recalled Due to Metal Contamination
Bakestone Brothers Pita Bread is being recalled due to the presence of metal pieces in the product. Consumers who have purchased this bread should not consume it and should discard it.
Product
Bakestone Brothers Pita Bread, 6 Whole Wheat Pitas. Net Wt. 11.4 oz(325g) UPC 0 57391-01002 6. Manufactured by PBF pita Bread Factory Ltd, 8000 Winston Street, Burnaby British Columbia V5A 2H5. Product of Canada
Category
Food
Distribution
5 states
HighFDA (Food)·F-0297-2025·2024-12-25
Bulk Candy Coated Popcorn Recalled for Undeclared Milk Allergen
Yoder's Cashew Crunch Corn, unlabeled bulk candy coated popcorn, is being recalled because milk allergen is not declared. The product was distributed to retail and wholesale locations in Iowa and Georgia.
Product
Yoder's Cashew Crunch Corn, bulk candy coated popcorn packaged in clear plastic without label.
Category
Food
Distribution
2 states
HighFDA (Food)·F-0374-2025·2024-12-25
Cucumber Products Recalled Due to Potential Salmonella Contamination
Indianapolis Fruit Company is recalling 288 cases of cucumber products distributed to Indiana, Kentucky, Ohio, and Pennsylvania due to potential salmonella contamination.
Product
Cucumbers Slices 1/2 Cup, 100 cups per case, Product Code CUCS100, Item Number - 14705 Cucumbers Diced 1" Peeled 5 lb. tray, 2 trays per case, Product Code CUDN45L, Item Number - 9975 Cucumbers Slices 2 oz., 100 per case, Product Code CUS100, Item Number - 9816 Cucumbers Slices
Category
Food
Distribution
4 states
HighFDA (Food)·F-0292-2025·2024-12-25
Whole Foods Organic Carrots & Celery Recalled Due to E. coli O121:H19 Contamination Risk
F&S Fresh Foods is recalling Whole Foods Market Organic Carrots & Celery due to potential E. coli O121:H19 contamination. The affected products were distributed in AZ, CA, HI, ID, and NV.
Product
WHOLE FOODS MARKET, Organic Carrots & Celery, NET WT. 15 oz (425 g), PERISHABLE KEEP REFRIGERATED, Packed For: Whole Foods Market Austin, TX 78703, Pre-washed and ready to eat
Category
Food
Distribution
5 states
HighFDA (Food)·F-0311-2025·2024-12-25
L'Oven Fresh KETO Tortilla Wraps recalled for possible metal contamination
Rise Baking Company is recalling L'Oven Fresh KETO Friendly Original 6 Tortilla Wraps sold at Aldi stores in five states due to potential metal contamination. Affected products carry specific Julian date codes from 24 302 to 24 311.
Product
L'Oven Fresh KETO Friendly Original 6 Tortilla Wraps. Net Wt. 7.8 oz(222g) UPC 4099100271348. Dist & Sold Exclusively By: Aldi, Batavia, IL 60510. Product of Canada
Category
Food
Distribution
5 states
HighFDA (Food)·F-0293-2025·2024-12-25
Yoder's Cashew Crunch hard candy recalled for undeclared milk allergen
Yoder's Cashew Crunch hard candy is being recalled due to undeclared milk allergen on the label. The product was distributed to retail and wholesale locations in Iowa and Georgia.
Product
Hard candy packed in clear plastic bag with gold/red label, Yoder's Cashew Crunch, Wt. 7oz, 2620 Hwy. 22, Riverside, IA 52327
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0710-2025·2024-12-25
Medical imaging software recall for incorrect DICOM orientation labels
Mint Lesion software versions 3.10.0 and 3.10.1 may display incorrect orientation labels for certain DICOM medical images. The defect affects 18 units distributed across the US and internationally.
Product
mint Lesion, Software Versions: 3.10.0 and 3.10.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0286-2025·2024-12-25
Food-Grade Salt Products Recalled for Foreign Material Contamination
Compass Minerals America Inc. is recalling approximately 67 metric tons of food-grade salt products due to foreign material contamination. The voluntary recall affects products distributed in Massachusetts, Indiana, Wisconsin, and Canada.
Product
Bulk salt product shipped in 1 metric ton tote; 50lb bag Special Purity Granulated Food-Grade Salt with UPC 041582150158; 44lb bag sifto Hy Grade Food Grade Salt, Compass Minerals America Inc. 9900 West 109th Street Overland Park, KS 99219
Category
Food
Distribution
3 states
HighFDA (Food)·F-0296-2025·2024-12-25
Candy coated popcorn recalled for undeclared milk allergen
Yoder's Cashew Crunch candy coated popcorn is recalled due to undeclared milk allergen on package labels. 319 packages were distributed to retail and wholesale locations in Iowa and Georgia.
Product
Candy coated popcorn packaged in clear plastic with gold label, 7 oz, Yoders Cashew Crunch Corn, 2620 Hwy. 22, Riverside, IA 52327
Category
Food
Distribution
2 states
HighFDA (Food)·F-0284-2025·2024-12-25
Impossible Savory Ground Sausage Recalled Due to Potential Metal Contamination
Impossible Foods is recalling Impossible Savory Ground Sausage nationwide due to potential metal contamination. Consumers should not consume affected products and should return them to their retailer.
Product
Impossible Savory Ground Sausage Meat from plants 14oz chub, UPC 8 16697 02108 8; 8 retail chubs per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0695-2025·2024-12-25
HUDSON RCI mBrace ET Tube Holder Risks Facial Dermal Injury
Medline is recalling the HUDSON RCI mBrace ET tube holder because defective adhesive and frame elements may cause pressure and skin injury to the face.
Product
HUDSON RCI mBrace, ET Tube Holder and 2 Point Head Strap, REF DYNJMBRC2; tracheal tube fixation device
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0687-2025·2024-12-25
K-Systems G73 Dry Bath Incubator may exceed target temperature
CooperSurgical is recalling K-Systems G73 Dry Bath Incubators because warming surfaces may exceed the desired set temperature. The device alarms when this occurs.
Product
Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes and embryos), at c
Category
Medical Device
Distribution
14 states
HighFDA (Drugs)·D-0142-2025·2024-12-25
FDA Recalls Health-Tec Benzocaine Topical Anesthetic Due to Manufacturing Defect
Keystone Industries recalls Health-Tec Topical Anesthetic (Benzocaine 20%) lot BNZ-001646 due to manufacturing defects. Scratches found in the mixing vessel caused product rejection designation, but product was inadvertently shipped.
Product
HEALTH-TEC TOPICAL ANESTHETIC — HEALTH-TEC TOPICAL ANESTHETIC (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0301-2025·2024-12-25
Artisan Multigrain Baguettes Recalled for Possible Metal Contamination
Stuyvers Bread is recalling Artisan Multigrain Baguettes (Lot #24313) due to possible metal contamination in a sub-ingredient. The product was distributed to two consignees in California, Connecticut, and Washington.
Product
Baguette, Artisan Multigrain. (30 Units/box) 400g/each. Contains: Wheat, Sesame Seeds, Gluten (rye, barley, oat) Lot#24313
Category
Food
Distribution
0 states
HighFDA (Food)·F-0295-2025·2024-12-25
Yoder's Cashew Crunch Hard Candy Recalled for Undeclared Milk Allergen
Yoder's Cashew Crunch hard candy is being recalled for undeclared milk allergen. The product was distributed in Iowa and Georgia to retail and wholesale customers.
Product
Yoder's Cashew Crunch, hard candy shipped in bulk in clear plastic bag.
Category
Food
Distribution
2 states
HighFDA (Food)·F-0300-2025·2024-12-25
Pull-Apart Holiday Rolls Recalled for Possible Metal Contamination
Stuyvers Bread is recalling Pull-Apart Holiday Rolls due to possible metal contamination in a sub-ingredient. The affected product was distributed to select retailers in California, Connecticut, and Washington.
Product
Pull apart Holiday Rolls (cluster bun). (2 Units/bag) 195g/each. Contains: Wheat, Milk Lot#24312
Category
Food
Distribution
0 states
ModerateFDA (Drugs)·D-0147-2025·2024-12-25
Benzocaine Topical Gel Recalled Due to Manufacturing Quality Defect
Keystone Industries recalls Ipana 20% Benzocaine Topical Gel due to a manufacturing quality issue. The bulk product was released from a mixing vessel with scratches despite Quality Unit rejection.
Product
Ipana, 20% Benzocaine Topical Gel, 28g, Maxill Inc., St Thomas ON Canada.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0145-2025·2024-12-25
Topical Anesthetic Gel Recalled for Manufacturing Process Deviation
Safco SensiCaine Ultra Topical Anesthetic Gel is being recalled due to a manufacturing process deviation. Product that should have been rejected because of damage to the mixing vessel was inadvertently released to customers.
Product
SAFCO SENSICAINE ULTRA TOPICAL ANESTHETIC GEL — SAFCO SENSICAINE ULTRA TOPICAL ANESTHETIC GEL (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0137-2025·2024-12-25
Benzocaine Topical Anesthetic Recalled for Manufacturing Equipment Defect
Gelato Benzocaine 20% topical anesthetic (Lot BNZ-001646) is recalled due to scratches found in the mixing vessel during manufacturing. The defective product was inadvertently released despite quality control rejection, though no illnesses have been reported.
Product
GELATO TOPICAL ANESTHETIC — GELATO TOPICAL ANESTHETIC (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0701-2025·2024-12-25
Augustine HOT DOG Temperature Management Controller Instructions Update
Augustine Temperature Management is issuing an instructions for use update for its HOT DOG warming controllers (Models WC77, WC77D, WC77R) regarding a power-on self-test error code.
Product
Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Multiport, Models: 1) Model # WC77, 2) Model # WC77D (Demo), 3) Model # WC77R (Refurbished); used in conjunction with Warming Blankets and Mattresses.
Category
Medical Device
Distribution
0 states
ModerateFDA (Drugs)·D-0154-2025·2024-12-25
Olanzapine 2.5 mg Tablets Recalled for Failed Impurity Specifications
Macleods Pharmaceuticals is recalling Olanzapine 2.5 mg tablets nationwide due to failed impurities and degradation specifications. The recall affects one production lot distributed across the United States.
Product
OLANZAPINE — OLANZAPINE (OLANZAPINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0685-2025·2024-12-25
ECG Patch Recorder Serial Number Mismatch - Eclipse Mini
Spacelabs Healthcare is recalling the Eclipse Mini ECG patch recorder because incorrect serial numbers may be programmed into devices, causing a mismatch between the physical label and internal serial number.
Product
Eclipse Mini REF 98900 The Eclipse MINI Model 98900 is a portable non-invasive continuous ambulatory ECG patch recorder intended to record the patient s electrocardiogram.
Category
Medical Device
Distribution
21 states
ModerateFDA (Devices)·Z-0691-2025·2024-12-25
K-Systems R65 embryo incubator temperature may exceed setpoint
CooperSurgical's K-Systems R65 Trolley reproductive incubators may experience temperature excursions above desired setpoints, though devices will alarm when this occurs. The FDA issued a Class II recall of 43 units across eight U.S. states.
Product
Brand Name: K-Systems Product Name: R65 Trolley Model/Catalog Number: K24012 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes and em
Category
Medical Device
Distribution
14 states
ModerateFDA (Devices)·Z-0699-2025·2024-12-25
Femoral Knee Prosthesis Components May Have Incorrect Packaging
MicroPort Orthopedics recalls EVOLUTION MP femoral knee prosthesis components due to incorrect packaging. The devices are correctly marked internally but may have wrong labels on their packaging.
Product
EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthesis component
Category
Medical Device
Distribution
0 states

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9701–9725 of 31231