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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applicatio
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic application
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applicatio
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in urological applicatio
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Hazard: Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
March 4, 2026Medical DevicesFDA
MRIMed Inc. recalls MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with
Hazard: Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION, Model Number: DYKM1361A; 2) TRUNK KIT 1EA, Model Number: DYKM201
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride), 7.1 FL OZ (21
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha recalls Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR
Hazard: Software anomaly in the patient positioning system may result in positional discrepancy.
March 4, 2026Medical DevicesFDA
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha recalls Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR
Hazard: Software anomaly in the patient positioning system may result in positional discrepancy.
March 4, 2026Food & BeverageFDA
SLADE GORTON & CO., INC. recalls Wellsley Farms Farm- Raised Atlantic Salmon Net WT. 32 oz. (2 lbs.) 907 g
Hazard: Contaminated with Listeria monocytogenes
March 4, 2026Food & BeverageFDA
Valley Springs Artesian Gold, LLC recalls Valley Springs Steamed Distilled Water. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-00601 2. Bottled by Valley Springs/Artesia
Hazard: Water was bottled under insanitary conditions.
March 4, 2026Food & BeverageFDA
Valley Springs Artesian Gold, LLC recalls Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-01301 0. Bottled by Va
Hazard: Water was bottled under insanitary conditions.
March 4, 2026Food & BeverageFDA
Valley Springs Artesian Gold, LLC recalls Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug with plastic caps: 1. 1 Gal Net
Hazard: Water was bottled under insanitary conditions.
March 4, 2026Food & BeverageFDA
Navitas, LLC. recalls NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA).
Hazard: Potential contamination with Salmonella.
March 4, 2026Food & BeverageFDA
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING recalls Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320
Hazard: Undeclared allergen ingredient (Wheat and Sesame)
March 4, 2026Food & BeverageFDA
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING recalls Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 810093891325
Hazard: Undeclared allergen ingredient (Wheat and Sesame)
March 4, 2026Food & BeverageFDA
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING recalls Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 810093891338
Hazard: Undeclared allergen ingredient (Wheat and Sesame)
March 4, 2026Food & BeverageFDA
SB FOOD LLC recalls Yoyo Gummy Grape Plus Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
Hazard: The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
March 4, 2026Food & BeverageFDA
SB FOOD LLC recalls Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
Hazard: The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
March 4, 2026Food & BeverageFDA
SB FOOD LLC recalls Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
Hazard: The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
March 4, 2026Food & BeverageFDA
TENGEN USA TRADING CORP recalls YO!MAN LETTUCE (SPICY FLAVOR); Ingredients: Lettuce, chili pepper, edible vegetable oil, salt, water, sugar, food additi
Hazard: Product contains undeclared cyclamates.