The Recall Desk

Archive

December 2025 recalls

744 recalls were announced in December 2025.

What the numbers show

Critical
102
Severe
54
High
363
Moderate
217
Low
8

Of the 744 recalls this month scored against our rubric, 14% are Critical, 7% are Severe.

Which agencies issued them

201–300 of 744

  • CriticalFDA (Food)·H-0316-2026·2025-12-17

    Bagged peaches recalled over potential Listeria monocytogenes contamination

    Moonlight Packing is recalling 46,048 cases of 2 lb bagged peaches, including Kroger-distributed packs, over potential contamination with Listeria monocytogenes.

    Product
    UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g DISTRIBUTED BY MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 0 11110 18174 9 PEACHES PRODUCE OF USA NET WT 32 OZ (2 LB) 907g DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0264-2026·2025-12-17

    Frozen ginger garlic cubes recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen ginger garlic 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 Ginger Garlic of India Net Wt. 10 oz. (283 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0251-2026·2025-12-17

    Frozen red pearl onions recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen red pearl onions after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Baby Bhindi KEEP FROZEN Net Wt. 12 oz (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0254-2026·2025-12-17

    Frozen kantola recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen kantola after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Kantola KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • 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 (Drugs)·D-0218-2026·2025-12-17

    Frozen jamun recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen jamun after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    LANTHANUM CARBONATE — LANTHANUM CARBONATE (LANTHANUM CARBONATE)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0293-2026·2025-12-17

    Frozen aviyal mix recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen aviyal mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Aviyal Mix KEEP FROZEN Net Wt. 14.1 oz. (400 g)
    Category
    Food
    Distribution
    0 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 (Drugs)·D-0225-2026·2025-12-17

    Frozen garlic cloves recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen garlic cloves after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0252-2026·2025-12-17

    ErgoStar CM 40 airway connectors recalled after cracks formed in the hose

    Draeger is recalling 14,420 ErgoStar CM 40 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
    Deep-brand Premium Select Chikoo Slices KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0282-2026·2025-12-17

    Frozen cooked water chestnuts recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen singoda water chestnuts after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Singoda (Cooked) Water Chestnuts Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0258-2026·2025-12-17

    Frozen punjabi tinda recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen punjabi tinda after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Punjabi Tinda KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0222-2026·2025-12-17

    Frozen chopped methi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen chopped methi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    NEBIVOLOL — NEBIVOLOL (NEBIVOLOL HYDROCHLORIDE)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0267-2026·2025-12-17

    Frozen val papdi recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen val papdi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Select Val Papdi Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0904-2026·2025-12-17

    Frozen mixed vegetables recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen mixed vegetables after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0237-2026·2025-12-17

    Oven dried fish recalled over Clostridium botulinum in uneviscerated fish

    African Food on Wheels is recalling 20 boxes of oven dried fish over Clostridium botulinum in uneviscerated fish. The FDA has classified the action as Class I.

    Product
    Oven Dried Fish (SCOMBEROMORUS CAVALLA); distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only; Product is packed in a corrugated brown box.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-0902-2026·2025-12-17

    Frozen baby bhindi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen baby bhindi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS
    Category
    Food
    Distribution
    1 state
  • 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
  • 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-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 (Food)·H-0319-2026·2025-12-17

    Peppermint peaches in count packs recalled over potential Listeria contamination

    Moonlight Packing is recalling 439 bags of 4-count Peppermint Peach packs over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.

    Product
    UPC 8 98429 00266 4 Peppermint Peach PROUCE OF U.S.A. 4 COUNT MIN. WT. 2.25 LBS MOONLIGHT PACKING CORPORATION REEDLEY, CA 93654
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0278-2026·2025-12-17

    Frozen green channa recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen green channa after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Green Channa Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0266-2026·2025-12-17

    Frozen sliced carrots recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen sliced carrots after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Select Carrots Sliced Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0271-2026·2025-12-17

    Frozen karela ring cut recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen karela ring cut after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Select Tindora Net Wt. 1 LB 8 oz. (24 oz.) (680 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0275-2026·2025-12-17

    Frozen tuvar lilva 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. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0322-2026·2025-12-17

    Frozen sambhar mix recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen sambhar mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Sticker label (for Loose Bulk - white peaches): 4401
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0295-2026·2025-12-17

    Frozen yellow turmeric haldi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen turmeric haldi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Turmeric Yellow Haldi KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0261-2026·2025-12-17

    Frozen green peas recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen green peas after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Suran Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0239-2026·2025-12-17

    Chocolate chip cookie dough recalled over possible Salmonella contamination

    Hudson River Foods is recalling 113 units of Doughy brand Chocolate Chip Cookie Dough because the product may be contaminated with Salmonella. The FDA has classified the action as Class I.

    Product
    Doughy brand Chocolate Chip Cookie Dough; 12 oz
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0274-2026·2025-12-17

    Frozen cut French beans recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen fansi cut French beans after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Fansi Cut French Beans Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0315-2026·2025-12-17

    Peppermint peaches in four pound packs recalled over potential Listeria contamination

    Moonlight Packing is recalling 13,069 cases of 4 lb Peppermint Peach white peaches over potential contamination with Listeria monocytogenes.

    Product
    UPC 8 10248 03087 1 Peppermint Peach WHITE PEACHES READY TO EAT FROM CALIFORNIA PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 8 10248 03163 2 Peppermint Peaches WHITE PEACHES READY TO EAT FROM CALIFORNIA PRODUCE OF U.S.A. NET WT. 4 LBS. M
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0273-2026·2025-12-17

    Loose bulk yellow peaches recalled in a second Listeria monocytogenes action

    Moonlight Packing is recalling a further 102,455 cases of loose bulk yellow peaches over potential contamination with Listeria monocytogenes, under FDA Class I.

    Product
    Deep-brand PREMIUM Select Hot Green Chillies Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0292-2026·2025-12-17

    Frozen diced tapioca recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen diced tapioca after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Tapioca (Cassava) Diced KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0287-2026·2025-12-17

    Frozen red guava slices recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen red guava slices after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Red Guava Slices KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0280-2026·2025-12-17

    Frozen ring cut lotus root recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen lotus root after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Lotus Root (Ring Cut) Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0899-2026·2025-12-17

    Frozen suran recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen suran after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-0590-2026·2025-12-17

    Frozen chikoo slices recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen chikoo slices after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    ErgoStar CM 40 Model/Catalog Number: MP01840 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
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·H-0288-2026·2025-12-17

    Frozen amla slices recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen amla slices after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Amla Slices KEEP FROZEN Net Wt. 10 oz. (283 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0253-2026·2025-12-17

    Frozen guvar recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen guvar after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Guvar KEEP FROZEN a) Net Wt. 12 oz. (340 g); b) Net Wt. 2 LB (907 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0301-2026·2025-12-17

    Frozen garlic quick cubes recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen garlic quick 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 Garlic of India KEEP FROZEN Net Wt. 10 oz. (283 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-0321-2026·2025-12-17

    Frozen hot green chillies recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen hot green chillies after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Sticker label (for Loose Bulk - yellow peaches): 4044
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0298-2026·2025-12-17

    Frozen diced green mango recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen diced green mango after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Diced Green Mango KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0314-2026·2025-12-17

    Packaged yellow peaches recalled over potential Listeria monocytogenes contamination

    Moonlight Packing is recalling 483,973 cases of 4 lb packaged yellow peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.

    Product
    UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 8 98429 00220 6 YELLOW Peaches from California PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0291-2026·2025-12-17

    Frozen diced bottle gourd recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen diced bottle gourd after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Dudhi (Lauki) Diced Bottle Gourd KEEP FROZEN Net Wt. 12 oz. (340 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-0269-2026·2025-12-17

    Frozen chauri recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen chauri after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Select Chauri 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-0318-2026·2025-12-17

    Peppermint peaches recalled over potential Listeria monocytogenes contamination

    Moonlight Packing is recalling 570 cases of 2 lb Peppermint Peach bags over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.

    Product
    UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORPORATION REEDLEY, CA 93654
    Category
    Food
    Distribution
    39 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 (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-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-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 (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
  • SevereNHTSA·25V872000·2025-12-17

    Toyota Highlander third row seat belt anchor may be installed incorrectly

    Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row centre seat belt roof anchor may have been installed at an incorrect angle.

    Product
    TOYOTA — TOYOTA HIGHLANDER HYBRID, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V875000·2025-12-17

    Autocar Recalls 2024 E-ACTT Tractor for Battery Cable Fire Risk

    Autocar is recalling one 2024 E-ACTT terminal tractor because improperly secured battery cable connections may overheat and cause a fire or loss of motive power.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V876000·2025-12-17

    Wheelchair restraint retractors in converted vans may fail to lock

    Rollx Vans is recalling certain converted vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints, because the retractors may not lock and the wheelchair may not be properly secured.

    Product
    HONDA — HONDA, TOYOTA, FORD ODYSSEY, SIENNA, TRANSIT, EXPRESS 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V873000·2025-12-17

    Suzuki Recalls 2025-2026 DR-Z400 Motorcycles for Brake Fluid Leak Risk

    Suzuki is recalling 2025-2026 DR-Z400S and 2025 DR-Z400SM motorcycles because incorrectly tightened screws may allow brake fluid to leak, reducing braking ability.

    Product
    SUZUKI — SUZUKI DR-Z400SM, DR-Z400S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V871000·2025-12-17

    BMW Recalls 2014-2015 Models Due to Head Air Bag Inflator Defect

    BMW is recalling specific 2014-2015 2, 3, and 4 Series vehicles because the head air bag inflator may fail, posing an injury risk during a crash.

    Product
    BMW — BMW M235I, 228I, 328I, 320I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0226-2026·2025-12-17

    Cinacalcet 90 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 12,576 bottles of Cinacalcet Hydrochloride Tablets, 90 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0898-2026·2025-12-17

    Fabric bandages recalled over open package seals affecting product sterility

    Medline is recalling 182,526 CURAD Germ-Shield Touch-Free Fabric Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box, Medline Item Number CUR1930F
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·H-0281-2026·2025-12-17

    Quick Strip fabric bandages, 1 by 3 inch, recalled over open seals

    Medline is recalling 11,291,800 Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Deep-brand PREMIUM Select Garlic Cloves Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0245-2026·2025-12-17

    Frozen potato gems recalled over semi-rigid plastic fragments embedded inside

    JR Simplot is recalling 7,053 cases of Simplot Traditional Reduced Sodium Tater Gems after pieces of semi-rigid plastic were found embedded in the product.

    Product
    Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes, 6/5lb bags per case, foodservice item, master case UPC 100 71179 00418 9. Distributed by Simplot Global Food, LLC, P.O. Box 9386, Boise, ID 83707
    Category
    Food
    Distribution
    19 states
  • HighNHTSA·25V877000·2025-12-17

    Chrysler Pacifica wheelchair restraints may not lock securely

    Vantage Mobility is recalling 2021–2025 Chrysler Pacifica vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may fail to lock, allowing wheelchairs to move unsecured during transit.

    Product
    TOYOTA — TOYOTA, HONDA, CHRYSLER SIENNA HYBRID, ODYSSEY, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0890-2026·2025-12-17

    Adhesive bandages recalled over open package seals that may compromise sterility

    Medline is recalling 1,566,500 Fur Friends Plastic Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, right, modular, L= 68 mm, Taper 10/12. Knee component of limb salvage replacement devices.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0903-2026·2025-12-17

    Quick Strip fabric bandages recalled over open seals affecting sterility

    Medline is recalling 6,989,900 Quick Strip Fabric Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25650QS
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0901-2026·2025-12-17

    Quick Strip plastic bandages recalled over open seals affecting sterility

    Medline is recalling 4,381,400 Quick Strip Plastic Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0597-2026·2025-12-17

    Fluoroscopy systems recalled after shipping without the source-to-skin distance spacer

    Philips is recalling 110 Azurion R3.0 systems shipped with a FlexArm stand but without the Source-to-Skin Distance spacer needed to meet the FDA minimum 38 cm requirement.

    Product
    Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0268-2026·2025-12-17

    Curad Quick Strip fabric bandages recalled over compromised package seals

    Medline is recalling 18,000 units of Curad Quick Strip Fabric Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Deep-brand Select Arvi Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0900-2026·2025-12-17

    Quick Strip plastic bandages, three quarter inch, recalled over open seals

    Medline is recalling 1,725,600 Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·H-0284-2026·2025-12-17

    Cinacalcet 60 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 15,744 bottles of Cinacalcet Hydrochloride Tablets, 60 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    Deep-brand PREMIUM Select Mixed Vegetables 4 way KEEP FROZEN a) Net Wt. 3.85 LB. (1.75 kg); b) Net Wt. 2 LB (907 g)
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0887-2026·2025-12-17

    Drainage catheter trays recalled over safety indicators showing the wrong position

    Bard Peripheral Vascular is recalling 1,240 Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator can show the catheter in the sharp position when it is blunt.

    Product
    Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V874000·2025-12-17

    Kia Sportage instrument panel screen may fail due to software error

    Kia is recalling certain 2023-2025 Sportage and Sportage Plug-In Hybrid vehicles with a 4.2-inch screen and a Kia tow hitch harness, because a software error may make the instrument panel screen fail.

    Product
    KIA — KIA SPORTAGE, SPORTAGE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0303-2026·2025-12-17

    Decaf coffee pods recalled because the boxes contained caffeinated pods

    Gimme Coffee is recalling 252 boxes of gimme! Decaf de Agua coffee pods because the outer packaging is labelled decaf while the pods inside are caffeinated Deep Disco pods.

    Product
    Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods Inner-packaging/pod packaging: gimme! coffee Deep Disco caffeinated coffee pods
    Category
    Food
    Distribution
    10 states
  • HighFDA (Drugs)·D-0224-2026·2025-12-17

    Cinacalcet 30 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0227-2026·2025-12-17

    Sertraline tablets recalled because bottle seals are not adhering

    Lupin Pharmaceuticals is recalling 52,128 bottles of Sertraline Hydrochloride Tablets, 100 mg, over a defective container in which the seal is not adhering to the bottles.

    Product
    SERTRALINE HYDROCHLORIDE — SERTRALINE HYDROCHLORIDE (SERTRALINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0896-2026·2025-12-17

    Titanium spinal spacers recalled over labeling claims not consistently present

    Orthofix U.S. is recalling 40,956 CONSTRUX Mini Ti Spacer System units because the labeling contains claims that are not consistently present.

    Product
    Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6006SP 12mm W X 12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0919-2026·2025-12-17

    Hospital mattresses recalled because they are not tested with certain beds

    Stryker is recalling 297 Arise 1000EX mattresses because they and certain MV3 beds have been sold in close proximity, and the two products have not been tested for compatibility.

    Product
    Stryker Arise 1000EX mattress, Part Number 2236000000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0255-2026·2025-12-17

    Knee fusion nail components recalled over a locking screw inserted backwards

    Waldemar Link is recalling 18 Endo Model Knee Fusion Nail SK coupling components delivered with a preassembled locking screw inserted from the wrong side into the male taper.

    Product
    Deep-brand Premium Select Karela Ring Cut KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0220-2026·2025-12-17

    Ganirelix acetate injection recalled after failing an impurity specification

    Lupin Pharmaceuticals is recalling 32,736 units of Ganirelix Acetate Injection after out of specification results for the ganirelix acetate acrylic acid adduct impurity.

    Product
    GANIRELIX ACETATE — GANIRELIX ACETATE (GANIRELIX ACETATE)
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0905-2026·2025-12-17

    Short ureteral stent kits recalled over a size labeling discrepancy

    C.R. Bard is recalling 116 Bard InLay Optima Ureteral Stent Kits, 6 Fr x 14 cm, because the actual stent size may not match the product label.

    Product
    Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0223-2026·2025-12-17

    Morphine sulfate oral solution recalled over a carton size mismatch

    Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0912-2026·2025-12-17

    Hemodialysis systems recalled because a screw may loosen or fall out

    Nipro Medical is recalling Surdial DX Hemodialysis Systems because a screw may loosen or fall out of the system.

    Product
    Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0217-2026·2025-12-17

    Lanthanum carbonate tablets recalled in a second hardness specification failure

    Cipla USA is recalling 1,180 boxes of Lanthanum Carbonate chewable tablets, 1000mg, from a further lot after an out of specification hardness test result.

    Product
    LANTHANUM CARBONATE — LANTHANUM CARBONATE (LANTHANUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0262-2026·2025-12-17

    Washer disinfectors recalled because a wire may shift causing internal arcing

    Steris is recalling 22 AMSCO 7053HP Washer/Disinfectors because a wire connected to the electrical box may shift out of position, which may result in electrical arcing inside the unit.

    Product
    Deep-brand Premium Select Surti Papdi Whole Net Wt. 12 oz. (340g) KEEP FROZEN
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0219-2026·2025-12-17

    Varenicline tablets recalled after an assay value fell below specification

    Dr. Reddy's Laboratories is recalling 4,800 bottles of Varenicline Tablets, 1mg, after the assay value for the affected lot fell below the specification limit at nine-month stability testing.

    Product
    VARENICLINE TARTRATE — VARENICLINE TARTRATE (VARENICLINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide

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