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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) GENERAL LAPAROSCOPY, Model Number: CDS930027Y
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ENT PACK, Model Number: DYNJ59030B; 2) ENT, Model Number: DYNJ908586C; 3) LH 3 PORT W/O WASTEBAG,
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model Number: DYNJ37543A
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) PICC TRAY, Model Number: DYNJ41648A
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) MTS LEFT HEART KIT-CAROLINAS HOS, Model Number: 60021775; 2) DBD-MTS LHK BHS BAPTIST. LOUISVI, Model
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF,
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK, Model Number: DYNJT2021G; 3) ANGIOGR
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB; 2) MANIFOLD KIT LOW PRESSURE OFF, Model N
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT, Model Number: DYNJ24517D
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Syringes: 1) SYRINGE 12ML CONTROL W/ROTATOR, Model Number: DYNJSYR12CWR; 2) SYRINGE 10ML CONTROL W/ROTATOR, M
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Namic Syringes: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB;
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM AN
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.
Hazard: Software issue that renders the touch screen unresponsive.
April 29, 2026Medical DevicesFDA
Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The
Hazard: In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
April 29, 2026Medical DevicesFDA
Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission
Hazard: In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
April 29, 2026Food & BeverageFDA
Costco Wholesale Corporation recalls Kirkland Signature Traditional Madeleines 12 Count/net wt. 18oz., Item #2000012, UPC 000020000127. Plastic clamshell con
Hazard: Undeclared hazelnut and soy lecithin.
April 29, 2026Food & BeverageFDA
Marquez Brothers International, Inc. recalls EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY ***
Hazard: Undeclared milk.
April 29, 2026Food & BeverageFDA
Marquez Brothers International, Inc. recalls EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE
Hazard: Undeclared milk.
April 29, 2026Food & BeverageFDA
Marquez Brothers International, Inc. recalls Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547
Hazard: Undeclared milk.
April 29, 2026Food & BeverageFDA
Summit Import Corporation recalls Spice Powder, 4 oz, Plastic Bag
Hazard: Lead level was higher than NYSAGM Standard.
April 29, 2026Food & BeverageFDA
Ethnic Foods Inc recalls Bombay Kitchen brand Punjabi Mix; Net Wt 9oz (255g); INGREDIENTS: Chickpea Flour, Water, Non-GMO Expeller Pressed Canola
Hazard: Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
April 29, 2026Food & BeverageFDA
Ethnic Foods Inc recalls Bombay Kitchen brand Tikka Sev; Net Wt 9oz (255g); INGREDIENTS: Chickpea Flour, Water, Non-GMO Expeller Pressed Canola O
Hazard: Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
April 29, 2026Food & BeverageFDA
Mondelez Global Llc recalls CHIPS AHOY! Baked Bites Brookie .22.4 oz Carton ( 2.8 oz pouch ) and 7.7 oz Carton ( 1.4 oz pouch)
Hazard: Hard corn starch lumps were found in the product
April 29, 2026Food & BeverageFDA
Unistel Industries Inc. recalls SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel Industries 650 Blossom Road Rochester, NY 14610; UPC: 7 69203
Hazard: Product may be contaminated with Salmonella.
April 29, 2026DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister packs
Hazard: Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin
April 29, 2026DrugsFDA
B BRAUN MEDICAL INC recalls LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC:
Hazard: Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
April 29, 2026DrugsFDA
B BRAUN MEDICAL INC recalls 0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524,
Hazard: Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
April 29, 2026DrugsFDA
B BRAUN MEDICAL INC recalls DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC:
Hazard: Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
April 29, 2026DrugsFDA
B BRAUN MEDICAL INC recalls Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 1801
Hazard: Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
April 29, 2026DrugsFDA
The Harvard Drug Group LLC recalls Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Pac
Hazard: Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.