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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Floor mounting column TruSystem 7500, Product Code 1717021
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Stationary column TruSystem 7500, Product Code 1717020
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Operating table column TS7500 MOBIUS, Product Code 1704695
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Premier Dental Products Co recalls Premier Solo Diamond - Large Invented Cone; SKU: 807016C.
Hazard: The hardness not meeting the material specification and may cause the diamond bur to bend.
April 2, 2025Medical DevicesFDA
Calyxo, Inc. recalls CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of urina
Hazard: Aspiration system, for endoscopic examination/treatment of urinary tract and kidney interior, to have labeling update adding additional instructions, for patients with high viscosity fluid in the kidney, not to continue providing fluid inflow in the presence of unresolved slow or absent fluid outflow because this can create intrarenal pressure imbalance, and lead to excessive intrarenal pressure.
April 2, 2025Medical DevicesFDA
Covidien recalls Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula, REF: 7CN80R
Hazard: Tracheostomy tube with cuff reusable inner cannula has a flange that may disconnect from the outer cannula of the device, which could cause respiratory failure, aspiration, unspecified tissue injury, aspiration, respiratory tract infection, bronchospasm, a delay to treatment and/or death.
April 2, 2025Food & BeverageFDA
Liaoning Cheng Da (USA) Inc recalls Wangzhine branded Hot Pot Sauce (SPICY); Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001382
Hazard: (Imported) Hot Pot Sauce (SPICY) contains undeclared allergens (Wheat and Soy)
April 2, 2025Food & BeverageFDA
Liaoning Cheng Da (USA) Inc recalls Wangzhine branded Hot Pot Sauce; Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001375
Hazard: (Imported) Hot Pot Sauce contains undeclared allergens (Wheat and Soy)
April 2, 2025Food & BeverageFDA
Veridance Pharmacal, LLC recalls Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per day with meals, Distr
Hazard: Levels of iodine exceeding label claim
April 2, 2025Food & BeverageFDA
Paletas Ice Cream, LLC recalls Flor de Michoacan Blue Hawaiian Artificially Flavored Beverage Concentrate. 1 Gallon (3.78L) Pasteurized. Keep Frozen
Hazard: Undeclared Red #3
April 2, 2025Food & BeverageFDA
Kenover Marketing Corp. recalls Glicks Dark Chocolate Conettos, 2.47 oz., Plastic Bag, 24 packages per case
Hazard: Undeclared Allergen (Milk)
April 2, 2025Food & BeverageFDA
U.S. Tov, Inc. dba U.S. Trading Company recalls DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING
Hazard: Undeclared sulfites
April 2, 2025Food & BeverageFDA
Dessert Holdings Llc recalls favorite day gourmet New York-Style CHEESECAKE 2 SLICES NET WT 6OZ (170 g) UPC 0 85239 09690 1 Target Brands, Inc.
Hazard: Undeclared Pecan. The firm was notified by their customer that when they were placing the product on the shelves, they noticed the wrong product was in the container.
April 2, 2025Food & BeverageFDA
Massimo Zanetti Beverage USA recalls COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g
Hazard: Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
April 2, 2025Food & BeverageFDA
Great Lakes Coca-Cola Distribution LLC recalls Coco-Cola Original Taste, 12 Fl Oz. (355mL). Can UPC 0 49000-00634 6. 12-can pack UPC 0 49000-02890 4. Canned Under A
Hazard: Foreign object (plastic)
April 2, 2025Food & BeverageFDA
HAR Maspeth Corp. recalls Jinga Glass Noodles with vegetables 8 oz. and 12 oz.
Hazard: Contains undeclared egg
April 2, 2025DrugsFDA
Exela Pharma Sciences LLC recalls 8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL (1 mEq/mL), 25 x 50 mL Single Dose Vials per carton, For Intravenou
Hazard: Lack of Assurance of Sterility
April 2, 2025DrugsFDA
Consumer Product Partners, LLC recalls [CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution, USP, 32 FL OZ (1 QT) 946 mL per bottle, NDC 0869-0871-45; [INC
Hazard: Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
April 2, 2025DrugsFDA
Ascent Consumer Products Inc. recalls SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-coun
Hazard: Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
April 2, 2025DrugsFDA
Ascent Consumer Products Inc. recalls SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg) for Nasal Wash Syste
Hazard: Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
April 2, 2025DrugsFDA
Ascent Consumer Products Inc. recalls SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 3
Hazard: Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
April 2, 2025DrugsFDA
Johnson, S C and Son, Inc recalls babyganics, Sheer Blend, SPF 50 Mineral Sunscreen Fragrance Free (zinc oxide 20%), a) 1.7 FL OZ (50 mL) bottle, UPC 8100
Hazard: Failed stability specifications: during routine stability monitoring quality concerns were identified. Physical separation for ingredients was observed.
April 2, 2025DrugsFDA
QuVa Pharma, Inc. recalls fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine HCl 200 mg/100 mL (2 mg/mL), 100 ml in NS Yellow CADD FS
Hazard: Lack of Assurance of Sterility
April 2, 2025DrugsFDA
QuVa Pharma, Inc. recalls fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL), 100 ml in NS Yellow CA
Hazard: Lack of Assurance of Sterility
April 2, 2025DrugsFDA
QuVa Pharma, Inc. recalls fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine HCl 100 mg/100 mL (1 mg/mL), 100 ml in NS Yellow CADD FS
Hazard: Lack of Assurance of Sterility
April 2, 2025DrugsFDA
Strides Pharma, Inc. recalls Testosterone Gel 1%, 5 grams, 30 Unit-dose Packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Bruns
Hazard: Presence of foreign substance: Presence of Benzene.
April 2, 2025DrugsFDA
Strides Pharma, Inc. recalls Testosterone Gel 1%, 2.5 grams, 30 Unit-dose packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Br
Hazard: Presence of foreign substance: Presence of Benzene.
April 2, 2025DrugsFDA
A-S Medication Solutions LLC recalls METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG, 180 TABLETS, Packaged BY: A-S Medication Solutions, Libertyville, IL 60
Hazard: Presence of Foreign Tablets/Capsules.
April 2, 2025VehiclesNHTSA
Entegra 2024–2025 Fuel System, Diesel recall
Hazard: A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
April 1, 2025VehiclesNHTSA
Bollinger Motors 2025 Electrical System recall
Hazard: Liquid intrusion into a battery pack can cause a loss of electrical isolation or short circuit, increasing the risk of a fire or shock hazard. In addition, the detection of a battery fault can cause a loss of drive power, increasing the risk of a crash.