Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,025 found- Use cautionMedical device
Philips North America Llc recalls BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended to produce images of the head and body. Model
Philips recalls Brilliance Volume CT scanners with model 728306 that may have a cooling unit expelling from the CT gantry, risking injury. Affected units include serial numbers 100100 and 100434.
PhilipsApr 13, 2021 - Lower riskDrug
Nomax Inc recalls Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of
Nomax recalls 100 sterile dry eye test strips (50 pouches) due to subpotent drug content. This may not provide proper eye test results. Consumers should contact Nomax for details.
NomaxApr 13, 2021 - Stop using nowFood
Mountain West Mothers' Milk Bank Inc. recalls Mountain West Mothers' Milk Bank - Pasteurized Donor Human Milk, 3 fluid ounce BPA free plastic bottles, embossed with
Mountain West Mothers' Milk Bank recalls specific batches of pasteurized donor human milk due to a foreign object found in the bottles.
Mountain West Mothers' Milk BankApr 13, 2021 - Lower riskFood
Snak King Corporation recalls Trader Joe's Restaurant Style White Corn Tortilla Chips; Net Wt. 9 oz. (255g)
Trader Joe's Restaurant Style White Corn Tortilla Chips (9 oz) may contain undeclared milk. Consumers should check packaging for recall dates and contact the manufacturer for details.
Snak KingApr 13, 2021 - Lower riskFood
Torn & Glasser, Inc. recalls Dark Chocolate Expresso Beans; Net Wt. 12 oz. (340g), Best if used by 11-19-2021. Contains Soy, May Contain Milk.
Torn & Glasser recalls Dark Chocolate Expresso Beans (12 oz) due to missing walnut allergen labeling. Product may contain peanuts, tree nuts, milk, wheat, and egg from shared equipment. Check UPC 072488998681 for affected lots.
Torn & GlasserApr 13, 2021 - Use cautionMedical device
Boston Scientific Corporation recalls VICI VENOUS STENT System Product Usage: is intended for the treatment of obstructions and occlusions in the venous
Boston Scientific recalls VICI Venous Stent System (May 2018-April 2021) due to reported stent migration after implantation. Affected patients should consult their doctor for evaluation.
Boston ScientificApr 12, 2021 - UnratedMedical device
DJ Orthopedics de Mexico S.A. de C.V. recalls DONJOY REF:11-0472-9 ULTRASLING PRO ER/IR 30, UNIVERSAL, Rx ONLY, UDI: (01)00190446683674 - Product Usage: intended for
DJ Orthopedics recalls specific DONJOY ULTRASLING PRO ER/IR 30 arm slings with a failed rivet at the chafe tab, which could cause injury during use. Affected units have UDI (01)00190446683674 and were sold in 2021.
DJ OrthopedicsApr 12, 2021 - Lower riskDrug
Edge Pharma, LLC recalls Betadine (Povidone-Iodine) 5%, 0.5mL per syringe Single Use Syringe Rx only, For Topical Ophthalmic Use (DO NOT INJECT)
Edge Pharma recalls Betadine 5% ophthalmic solution due to potential contamination from syringe migration. Affected lots from May 2021 may cause infection if used improperly.
Edge PharmaApr 12, 2021 - Lower riskDrug
Preferred Pharmaceuticals, Inc. recalls Cephalexin for Oral Suspension, Generic for Keflex, USP, Powder for Oral Suspension, 250 mg/5mL, Pkg Size 100, Rx only,
Preferred Pharmaceuticals recalls Cephalexin oral suspension (250mg/5mL) for potential impurities found during testing. This is a repackaged product from Ascend Laboratories. No immediate action needed as it's prescription-only.
Preferred PharmaceuticalsApr 12, 2021 - Lower riskFood
Ample Hills Manufacturing LLC. recalls Ample Hills Creamery Chocolate Milk and Cookies Ice Cream, 14 oz.
Ample Hills recalls 14oz chocolate milk and cookies ice cream due to undeclared soy lecithin and coconut oil. Consumers should check lot numbers on packaging for affected products.
Ample HillsApr 12, 2021 - Lower riskFood
Indiana Botanic Gardens, Inc recalls Botanic Choice Green Tea Leaf Extract (3:1 Extract), Alcohol Free Liquid Extract, 1 FLOZ., in glass jar with dropper,
Indiana Botanic Gardens recalls Botanic Choice Green Tea Leaf Extract due to incorrect active ingredient listed on product label. Affected items have UPC 70330:200164 and Lot 6102649.
Indiana Botanic GardensApr 12, 2021 - Lower riskFood
Backcountry Mills LLC recalls G4G Low Carb Pancake & Waffle Mix, Keto Friendly Just Add Water Net Wt 12 ounces, 6pack Case UPC 860000241427 packaged
Backcountry Mills recalls 6-packs of G4G Low Carb Pancake & Waffle Mix due to potential Salmonella contamination. Consumers should check product codes and contact the company for details.
Backcountry MillsApr 12, 2021 - Lower riskFood
NATURE'S SUNSHINE PRODUCTS recalls Love & Peas Protein Rich Meal Replacement, Sugar Free, 1 LB 9 OZ (713 G) bag, Nature's Sunshine Products, Inc., Spanish
Nature's Sunshine recalls Love & Peas Protein Rich Meal Replacement (Sugar Free) due to potential milk traces in vegan/dairy-free products. Consumers should check lot numbers and contact the company for details.
Nature's SunshineApr 12, 2021 - Stop using nowConsumer product

Black Diamond Recalls PIEPS DSP Avalanche Transceivers Due to Risk of Loss of Emergency Communications; One Death Reported
Black Diamond recalls PIEPS DSP Pro, Pro Ice, and Sport avalanche transceivers due to unexpected mode switching that can prevent emergency signals during avalanches, risking severe injury or death.
Black DiamondApr 12, 2021 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Raw Ground Turkey Products Linked to Salmonella Hadar Illness
USDA FSIS recalls approximately 211,406 pounds of Plainville Brands raw ground turkey products from December 2020 linked to Salmonella Hadar illness. Consumers urged not to consume these products.
Plainville BrandsApr 10, 2021 - Use cautionVehicle
NISSAN MURANO HYBRID (2016) recall — Engine And Engine Cooling
Nissan recalls 2016 Murano Hybrids with potential engine power loss causing crash risk. Owners must contact Nissan or Infiniti for free software update by March 31, 2022.
NissanApr 10, 2021 - Lower riskFood
HOSTESS BRANDS LLC recalls Hostesss SnoBalls packaged as Hostess Chocolate CupCakes, Net Wt 3.17 OZ, UPC 8 88109 01001 0, Hostess Brands, LLC
Hostess recalls SnoBalls packaged as Chocolate CupCakes due to failure to label coconut, a major food allergen. Consumers should check UPC 8 88109 01001 0 for affected products.
HostessApr 10, 2021 - Lower riskMedical device
SPINEART SA recalls PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft. Pediatric pedicle
SPINEART recalls PERLA TL Lateral Connector Open models with incorrect rod size labeling. Affected units may have wrong size labels, potentially causing improper spinal fixation in pediatric cases.
SPINEARTApr 9, 2021 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B
Medical Action Industries recalls LVAD dressing change kit (part 79544B) due to potential breach in BD ChloraPrep 3mL applicator packaging. Affected units were sold with specific lot numbers and expiration dates.
Medical Action IndustriesApr 9, 2021 - UnratedMedical device
INNOVA MEDICAL GROUP, INC. recalls COVID-19 Self-Test Kit *** INNOVA *** 3T
Innova recalls 3T COVID-19 self-test kits distributed outside clinical trials. This may pose risks if used by non-clinical participants. Affected kits have specific lot numbers.
InnovaApr 9, 2021 - Use cautionMedical device
Avid Medical, Inc. recalls FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.
Avid Medical recalls FISTULA ON-OFF Kit (Part MMTN020) due to potential Aspergillus contamination from package breaches. Affected kits may need replacement to prevent infection risks.
Avid MedicalApr 9, 2021 - Stop using nowDrug
Teligent Pharma, Inc. recalls Flurandrenolide Ointment USP, 0.05%, Net Wt. 60 grams, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310 NDC
Teligent Pharma recalls 0.05% Flurandrenolide Ointment (60g) due to failed impurities and degradation specifications. Rx-only product with NDC 52565-017-60, Lot #13974 exp 7/2021. Stop using immediately.
Teligent PharmaApr 9, 2021 - Use cautionVehicle
VOLKSWAGEN ID.4 (2021) recall — Seat Belts
Volkswagen recalls 2021 ID.4 vehicles with faulty rear seat belts that may not secure child restraints properly during crashes. Owners must have seat belts inspected and replaced if needed.
VolkswagenApr 8, 2021 - Use cautionVehicle
PORSCHE PANAMERA TURBO S (2021) recall — Seat Belts
Porsche recalls 2021 Panamera Turbo S vehicles with faulty seat belts that may not secure child restraints during crashes. Owners must have seat belts inspected and replaced free by dealers.
PorscheApr 8, 2021 - Use cautionVehicle
NEWMAR NEW AIRE (2021) recall — Fuel System, Diesel
Newmar is recalling 2021-2022 New Aire motorhomes with Cummins diesel engines due to potential fuel leaks that could cause fire if near ignition sources. Owners must contact customer service for free hose replacement.
NewmarApr 8, 2021 - Lower riskMedical device
Smith & Nephew, Inc. recalls CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of
Smith & Neph: Recall of 6mm x 30mm interference screws due to mislabeled box containing 6mm x 20mm screws. Affected users should check product details.
Smith & NephewApr 8, 2021 - Use cautionMedical device
Windstone Medical Packaging, Inc. recalls Angio Pack REF: AMS6908C, Sterile EO, Contents:1 Blade Scalpel # 11 SS 1 Bowl Guidewire 80 oz 4 Clamp Towel 2.5 1 Cover
Windstone Medical Packaging recalls 114 Angio Pack kits (REF AMS6908C) due to insufficient angio tubing welds. Check lot numbers 146304 and 147534.
Windstone Medical PackagingApr 8, 2021 - Lower riskMedical device
Meridian Bioscience Inc recalls Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse Transcription Polymerase Chain Reaction (rRT-PCR)
Meridian Bioscience recalls Revogene SARS-CoV-2 test (Catalog 410700) due to reported false negative results in emergency use. All units affected.
Meridian BioscienceApr 8, 2021 - UnratedMedical device
Spes Medica recalls SNS Disposable Urethral Catheter Electrode, 10 Fr, Gold Recording/Stimulating Contact printed on polyurethane film
Spes Medica recalls 10 Fr urethral catheter electrodes due to possible sterilization process deviations. Affected units have reference number UE006 and lot UR20F2702I. No remedy specified in official notice.
Spes Med: 10 Fr Catheter ElectrodeApr 8, 2021 - Stop using nowDrug
NSNY Distributor Inc recalls Ginseng Power 5000 capsule, 1- count per blister card, GS Natural Co, Los Angeles, CA 90010, UPC 0 40232 18144 3
NSNY Distributor Inc recalls Ginseng Power 5000 capsules due to undeclared sildenafil and tadalafil. These substances are not approved for use in dietary supplements.
GS Natural CoApr 8, 2021
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