Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,851 recalls, newest first · Checked 0 minutes ago
United StatesGalt Medical Corporation recalls Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP
Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits.Baxter Healthcare Corporation recalls Baxter Duo-Vent Solution Set and Male Luer Lock Adapter
Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position.Spectra Medical Devices, Llc recalls Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection
Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance.Terumo Medical Corporation recalls GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The…
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.Philips Medical Systems Nederland B.V. recalls Allura Xper FD. Model Numbers: 722026
Firmware issue potentially leading to loss of geometry movements.Medline Industries, LP recalls Medline Micro-Kill Bleach Germicidal Bleach Wipes and 3 more products
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month…Microvention Inc. recalls BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US…
Due to an increase rate of balloon pinhole defects.Covidien, LP recalls V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22… and 4 more products
Product may contain a perforation or tear in the sterile barrier packaging.Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT and 7 more products
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.W L Gore & Associates, Inc. recalls GORE VIABIL Short Wire Biliary Endoprosthesis and 1 more products
10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes…Baxter Healthcare Corporation recalls Cefazolin in Dextrose
Presence of Particulate MatterNovartis Pharmaceuticals Corporation recalls Diovan
Failed Dissolution SpecificationsPrestige Brands Holdings recalls CLEAR EYES Maximum Itchy Eye Relief
Lack of assurance of sterility.Heritage Pharmaceuticals Inc recalls CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.Liebel-Flarsheim Company LLC recalls Optiray Imaging Bulk Package-350
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.Victory Medical Center Pharmacy recalls Glutathione
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.Apollo Care, LLC recalls SEMAGLUTIDE 12.5MG and 10 more products
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type materialShoolin Pharma Chem LLP recalls SILDENAFIL CITRATE USP and 4 more products
CGMP Deviations:Noted during FDA inspectionBuy-Herbal recalls Kian Pee Wan Capsules
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.Piazza Produce (dba CIBUS Fresh) recalls Cibus Fresh
Possible Cyclospora Contamination529 Commerce, LLC recalls Aquafaba Powder
Undeclared EggSheandro LLC recalls Vodka Tomato Sauce
Label declares cream and cheese, but Milk is not declaredFlavorsandColor.Com recalls Honeyville YELLOW COLOR 1 GALLON NFI: WATER
Undeclared Red #40.A little guidance
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