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

176–200 of 7436

CriticalFDA (Devices)·Z-0914-2026·2025-12-24
Carestation 750 anesthesia systems recalled over potential unexpected shutdown
GE Medical Systems is recalling 888 Carestation 750 series anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The action is Class I.
Product
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012-9750-002; Carestation 750c A1, REF 1012-9755-000; Products for which affected PMB can be used as a spare part: Carestatio
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0913-2026·2025-12-24
Anesthesia systems recalled over potential unexpected shutdown on mains power loss
GE Medical Systems is recalling 1,277 Carestation anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The FDA has classified the action as Class I.
Product
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012-9620-000; Carestation 620 A1, REF 1012-9620-200; Carestation 620 A1, REF 1012-9620-202; Carestation 620 SE A1, REF 1012-9620
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0311-2026·2025-12-24
Dried salted smelts recalled over Clostridium botulinum in uneviscerated fish
MAMTAKIM is recalling 45 cases of Belevini Korushka dried salted whole smelts over Clostridium botulinum in uneviscerated fish. The FDA has classified the action as Class I.
Product
Belevini KORUSHKA, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK, 20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0325-2026·2025-12-24
Organic senna leaves recalled over potential contamination with Salmonella
The Whole Herb Company is recalling 3,580 lbs of organic cut and sifted senna leaves over potential Salmonella contamination. The FDA has classified the action as Class I.
Product
SENNA LEAVES F/C OG Item No: SEN15001 Net Wt: 44.75 Lbs Distributed By Whole Herb Company 19800 8th Street East, Sonoma, CA 95476 UPC 10031 44312
Category
Food
Distribution
2 states
CriticalFDA (Food)·H-0312-2026·2025-12-24
Dried salted bichki smelts recalled over Clostridium botulinum in uneviscerated fish
MAMTAKIM is recalling 4 cases of Belevini Bichki dried salted whole smelts over Clostridium botulinum in uneviscerated fish. The FDA has classified the action as Class I.
Product
Belevini BICHKI, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK,20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
Category
Food
Distribution
5 states
CriticalFDA (Devices)·Z-0915-2026·2025-12-24
Anesthesia power management boards recalled over potential unexpected system shutdown
GE Medical Systems is recalling 203 Carestation anesthesia system Power Management Board field replaceable units over potential unexpected shutdown if AC mains power is lost.
Product
GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-S
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0310-2026·2025-12-24
Organic supergreens powder mix recalled after contamination with Salmonella
Lexunder is recalling 159 units of Food to Live brand Organic Supergreens Powder Mix contaminated with Salmonella. The FDA has classified the action as Class I.
Product
Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 1.5 lb., 3 lb., 6 lb., 12 lb.; Ingredients: ORGANIC KALE; ORGANIC MORINGA LEAF; ORGANIC WHEAT GRASS; ORGANIC SPIRULINA UPC: 8 oz. - 810097461475 1 lb. - 8100974
Category
Food
Distribution
38 states
CriticalFDA (Food)·H-0300-2026·2025-12-17
Frozen pani puri stuffing recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen instant stuffing for pani puri after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand Instant Stuffing For Pani Puri KEEP FROZEN Net Wt. 1 LB. (454 g)
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-0593-2026·2025-12-17
ErgoStar CM 60 airway connectors recalled after cracks formed in the hose
Draeger is recalling 2,050 ErgoStar CM 60 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Product
ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
Category
Medical Device
Distribution
10 states
CriticalFDA (Food)·H-0249-2026·2025-12-17
Infant formula recalled after contamination with Clostridium botulinum
ByHeart is recalling 3,482,131 cans and 3,531,901 single serve packets of Whole Nutrition Infant Formula after contamination with Clostridium botulinum. The FDA has classified the action as Class I.
Product
1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams in packages containing 14 Single Serve Packets
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0592-2026·2025-12-17
ErgoStar CM 55 airway connectors recalled after cracks formed in the hose
Draeger is recalling 118,850 ErgoStar CM 55 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Product
ErgoStar CM 55, Model/Catalog Number: MP01855, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
Category
Medical Device
Distribution
10 states
CriticalFDA (Food)·H-0272-2026·2025-12-17
Frozen green chili cubes recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen green chili cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand Indian Kitchen Quick Cubes Ready For Cooking Green Chili of India Net Wt. 10 oz. (283 g) KEEP FROZEN
Category
Food
Distribution
0 states
CriticalFDA (Food)·H-0324-2026·2025-12-17
Loose bulk peppermint peaches recalled in a second Listeria monocytogenes record
Moonlight Packing is recalling a further 2,622 cases of loose bulk peppermint peaches over potential Listeria monocytogenes contamination, under enforcement record H-0324-2026.
Product
Sticker label (for Loose Bulk - peppermint peaches): 4401
Category
Food
Distribution
39 states
CriticalFDA (Food)·H-0299-2026·2025-12-17
Frozen ponk with tangy sev recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen ponk with tangy sev after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand Ponk With Tangy Sev KEEP FROZEN Net Wt. 6 oz. (170 g)
Category
Food
Distribution
0 states
CriticalFDA (Food)·H-0270-2026·2025-12-17
Frozen cut okra recalled after the product tested positive for Salmonella
Chetak New York is recalling Deep-brand frozen bhindi cut okra after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand Select Bhindi Cut Okra KEEP FROZEN a) Net Wt. 12 oz (340 g); b) Net Wt. 1 LB 8 oz. (24 oz.) (680 g); c) Net Wt. 2 LB (907 g)
Category
Food
Distribution
0 states
CriticalFDA (Food)·H-0294-2026·2025-12-17
Frozen green garlic recalled after the product tested positive for Salmonella
Chetak New York is recalling Deep-brand frozen green garlic after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand PREMIUM Select Green Garlic KEEP FROZEN Net Wt. 12 oz. (340 g)
Category
Food
Distribution
0 states
CriticalFDA (Food)·H-0260-2026·2025-12-17
Frozen tuvar lilva, 24 ounce bags, recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen tuvar lilva after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand Premium Select Tuvar Lilva Net Wt. 1 LB 8 oz. (24 oz.) (680 g) KEEP FROZEN
Category
Food
Distribution
0 states
CriticalFDA (Food)·H-0286-2026·2025-12-17
Frozen peas and carrots recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen peas and carrots after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand PREMIUM Select Peas and Carrots KEEP FROZEN Net Wt. 2 LB (907 g)
Category
Food
Distribution
0 states
CriticalFDA (Food)·H-0279-2026·2025-12-17
Frozen snake gourd recalled after the product tested positive for Salmonella
Chetak New York is recalling Deep-brand frozen snake gourd after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand PREMIUM Select Snake Gourd Net Wt. 12 oz. (340 g) KEEP FROZEN
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-0910-2026·2025-12-17
Frozen whole surti papdi recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen surti papdi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0246-2026·2025-12-17
Frozen arancini recalled over undeclared soy protein concentrate
Stuffed Foods is recalling 51 cases of Cacio e Pepe Arancini over undeclared soy protein concentrate. The FDA has classified the action as Class I.
Product
Stuffed Foods brand Cacio e Pepe Arancini; KEEP FROZEN; For institutional use only; Ready-to-cook; Cook to internal temp. of 165oF; Case pack: 3/3 lbs; Net Weight: 9lbs; UPC 00819985020787
Category
Food
Distribution
4 states
CriticalFDA (Food)·H-0256-2026·2025-12-17
Frozen methi blocks recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen methi blocks after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand Premium Select Methi Blocks KEEP FROZEN Net Wt. 12 oz. (340 g)
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-0892-2026·2025-12-17
Frozen surti undhiu mix recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen surti undhiu mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 7H 38-1008SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 8H; 38-1009SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 9H; 38-1010
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0283-2026·2025-12-17
Frozen arvi recalled after the product tested positive for Salmonella
Chetak New York is recalling Deep-brand frozen arvi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Product
Deep-brand PREMIUM Select Green Peas KEEP FROZEN a) Net Wt. 3.85 LB. (1.75 kg); b) Net Wt. 2 LB. (907 g)
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-0591-2026·2025-12-17
Ventilator airway connectors recalled after cracks formed in the hose
Draeger is recalling 191,470 ErgoStar CM 45 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Product
ErgoStar CM 45, Model/Catalog Number: MP01845, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
Category
Medical Device
Distribution
10 states

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176–200 of 7436