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
35,021 found- Use cautionMedical device
Shimadzu Medical Systems recalls Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan -
Shimadzu recalls Mobile X-Ray System (MX8) with adjustable handle option due to potential improper bolts causing unsafe operation. Affected units have specific SMS IDs listed.
ShimadzuNov 9, 2020 - Lower riskMedical device
Exactech, Inc. recalls Equinoxe Humeral Stem, Primary, Press Fit, 11mm
Exactech recalls 11mm Equinoxe Humeral Stems with potential for incorrect Instructions for Use. Affected units include specific serial numbers and packaging lots. Consumers should contact Exactech for details.
ExactechNov 9, 2020 - Lower riskMedical device
ROi CPS LLC recalls Custom procedure packs, containing banded 4x4 Raytec 16ply gauze sponges. 1) Regard, PACEMAKER, Item 800221010, Lot #
ROi CPS recalls custom procedure packs with banded 4x4 Raytec 16ply gauze sponges that may flake or fray. Affected items include specific models and lot numbers listed in the recall notice.
ROi CPSNov 9, 2020 - Lower riskFood
Mayer Brothers Apple Products, Inc. recalls 1. Giant brand " Premium Apple Cider*** 64 fl. oz. (Half Gal) 1.89L***Distributed by Foodhold USA LLC, Landover, MD
Mayer Brothers recalls 64 fl oz and 128 fl oz apple cider due to processing error mixing pasteurized and raw cider. Consumers should check UPC codes and lot numbers for affected products.
Mayer BrothersNov 9, 2020 - Lower riskMedical device
Bausch & Lomb Surgical, Inc. recalls MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is
Bausch & Lomb recalls MX60ET toric contact lenses due to possible missing toric axis marks. Affected lenses may not fit properly during eye surgery.
Bausch & LombNov 7, 2020 - Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls NaturaLyte Liquid Acid concentrate drums, Model Number 13-1251-1 - Product Usage: used in conjunction with Fresenius
Fresenius recalls NaturaLyte Liquid Acid concentrate drums (Model 13-1251-1) used in hemodialysis machines due to low sodium/calcium levels. Check lot numbers 20LXAC034, 20LXAC069, 20NXAC040 for affected units.
FreseniusNov 7, 2020 - Use cautionVehicle
JEEP CHEROKEE (2017) recall — Power Train
Chrysler recalls 2014-2017 Jeep Cherokees with power transfer unit issues that may cause loss of drive or unintended rollaway. Owners must get a software update to prevent crashes.
ChryslerNov 6, 2020 - Lower riskMedical device
Spacelabs Healthcare, Ltd. recalls Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is
Spacelabs Healthcare recalls Sentinel V10.x and V11.x models 98200/98201 after system upgrades may add incorrect comments to ECG and blood pressure tests, potentially causing confusion in results.
Spacelabs HealthcareNov 6, 2020 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative
Roche recalls Tina-quant C-Reactive Protein Gen 3 (catalog 0517237:42402301) due to low quality recovery and invalid calibrations from cross contamination between reagents.
RocheNov 6, 2020 - Lower riskDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls clomiPRAMINE Hydrochloride Capsules USP, 50 mg, 30-count bottle, Rx Only, Manufactured by: Jubilant Cadista
Jubilant Cadista is recalling 50mg clomipramine hydrochloride capsules (Rx only) because of failed tablet specifications. This recall affects specific lots manufactured in Salisbury, MD. Consumers should contact the manufacturer for details.
Jubilant CadistaNov 6, 2020 - Lower riskFood
The Kroger Co recalls HomeChef meal kit: Buffalo Pretzel Chicken Breast with Roasted Cauliflower and Broccoli. 29 ounce.
Kroger recalls HomeChef meal kits with Buffalo Pretzel Chicken Breast due to potential Listeria contamination in the pretzel breading. Consumers should check lot numbers and contact Kroger for details.
KrogerNov 6, 2020 - Use cautionFood
Quantum Inc recalls Quantum Health branded Elderberry liquid herbal extract dietary supplement is packaged in 2oz glass bottle, 12
Quantum Health recalls 12-bottle elderberry liquid supplement due to potential Salmonella contamination. Discard unused bottles to avoid foodborne illness risk.
Quantum HealthNov 6, 2020 - Lower riskFood
Singh Trading Inc. DBA Roshni Foods recalls Green Raisins 200 grams (7 oz.) Packaged in plastic bags. Bar Code:992203621
Roshni Foods recalls 200g green raisins (bar code 992203621) due to undeclared sulfites. Consumers should check packaging for batch 20020 and contact for details.
Roshni FoodsNov 6, 2020 - Stop using nowFood
Tanimura & Antle recalls Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura &
Tanimura & Antle recalls romaine lettuce with E. coli O157:H7 contamination found in Michigan. Products sold in the US with UPC 2-27918 20314-9 from October 15-16, 2020.
Tanimura & AntleNov 6, 2020 - Lower riskFood
Rosebud's Ranch and Garden, LLC recalls Rosebud's brand Elderberry Syrup Kit in a 3 oz. clear stand-up pouch (GS1 Code 852782007834).
Rosebud's Ranch recalls elderberry syrup kits with potential salmonella contamination. Consumers should check product codes and contact the company for details.
Rosebud'sNov 6, 2020 - Lower riskMedical device
VEO DIAGNOSTICS, LLC recalls ACCEL ELISA COVID-19 for the detection of total antibodies to SARS-CoV-2 Catalog AE301U Kit lots: PXCOV073020,
VEO Diagnostics recalls ACCEL ELISA COVID-19 antibody test kits (AE301U, lots PXCOV073020 and PXCOV081220) after FDA emergency use authorization was removed.
VEO DiagnosticsNov 5, 2020 - Lower riskMedical device
Medline Industries Inc recalls RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing per Tyvec Peel Pouch, 30 Pouches per
Medline recalls RevMedX Trauma Dressings due to potential package seal issues that may compromise sterility. Affected items include specific lot numbers from August 2022 to May 2023.
MedlineNov 5, 2020 - Lower riskMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)
Medtronic recalls specific Cobalt CRT-D defibrillators due to a potential manufacturing error in cathode components, though all devices passed functional tests.
MedtronicNov 5, 2020 - Lower riskDrug
Teligent Pharma, Inc. recalls Clobetasol Propionate Ointment USP 0.05%, Net Wt. 50 grams, Rx Only, Teligent Pharma. Inc. Buena, NJ 08310 NDC
Teligent Pharma recalls 50g Clobetasol Propionate Ointment USP 0.05% (Rx Only) due to inconsistent potency levels that may cause under or over treatment. Affected lots: 12597, exp. 12/2020.
Teligent PharmaNov 5, 2020 - Stop using nowFood
John Nagle Co. recalls John Nagle Steelhead Fillets; 1/3 lb; Iceland; N44515; Habrun ehf; Packaging date: 29 10 2020
John Nagle Co. recalls Steelhead Fillets due to potential Listeria monocytogenes contamination. Check your product details and packaging dates.
John NagleNov 5, 2020 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Spaghetti and Meatballs in Marinara Sauce Products Due to Possible Foreign Matter Contamination
FSIS public health alert: Spaghetti and meatballs in marinara sauce products may contain metal fragments. Consumers are urged not to consume these products, which were produced between Oct. 17-2020. No recall was requested as products are no longer available.
FSISNov 4, 2020 - Lower riskMedical device
K2M, Inc recalls Everest MI XT Tab Removal Tool (i.e. All-In-One Tab Removal Tool)-used to break the tab off the Everest XT screw by
K2M recalls Everest MI XT Tab Removal Tools due to cracking at the metal shaft and handle interface, which may cause Loctite leakage. Affected units have specific catalog and lot numbers.
K2MNov 4, 2020 - Stop using nowConsumer product
YETI Recalls Rambler Travel Mugs with Stronghold Lid Due to Injury and Burn Hazards
YETI recalls 20 oz Rambler Travel Mugs with Stronghold Lids due to magnet slider ejecting and hot liquids spilling, causing injury or burns. Affected units have date code 34204010.
YETINov 4, 2020 - Stop using nowConsumer product
Walker Edison Recalls Chests Due to Tip-Over and Entrapment Hazards
Walker Edison recalls drawer chests due to tip-over and entrapment hazards. Stop using immediately and contact the company for a refund or replacement.
Walker EdisonNov 4, 2020 - Stop using nowConsumer product
Target Recalls Toddler Boots Due to Choking Hazard
Target recalls Cat & Jack Himani and Jaren toddler boots (sizes 5-12) due to choking hazard from elastic lace toggle that can detach. Consumers should stop using and return for refund.
Cat & JackNov 4, 2020 - Stop using nowConsumer product
Coulter Ventures Recalls Rogue Home Timers Due to Fire Hazard; Sold Exclusively at Rogue Fitness
Rogue Home Timers recalled due to fire risk from lithium-ion batteries overheating. Consumers must stop using and get refunds.
RogueNov 4, 2020 - Stop using nowConsumer product
Alliance Outdoor Products Recalls Climbing Treestands Due to Fall Hazard
Alliance Outdoor recalls 2017 model climbing treestands due to cable corrosion causing fall hazards. Affected units include Silent Adrenaline XSCT334 and Apache XSCT355 with batch numbers ending in '17'. Consumers must stop using and get a refund gift card.
Alliance Outdoor ProductsNov 4, 2020 - Use cautionMedical device
NEOSTEO recalls Cannulated graduated drill bit 1.9 mm diameter, with AO QC system, REF: INS-114 for use in orthopedic surgery.
Neosteo recalls 1.9mm cannulated drill bits with AO QC system (lot 243-20) due to corrosion traces that may cause inflammation, pain, or allergic reactions during orthopedic surgery.
NeosteoNov 3, 2020 - Lower riskMedical device
Kowa Optimed Inc recalls Kowa VK-2s software Version 10.0.4.0, Product code 04987646809500 installed on Kowa nonmyd WX Retinal Cameras - Product
Kowa Optimed recalls specific retinal camera software versions that could delete patient information if multiple IDs are deleted simultaneously, causing treatment delays.
KowaNov 3, 2020 - Lower riskMedical device
K2M, Inc recalls Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Usage: The Anti-Torque Alignment Tube (the Alignment
K2M recalls Yukon Anti-Torque Alignment Tube (Lot KTGG) due to potential surgery delays. Affected users should contact K2M for details.
K2MNov 3, 2020
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,609 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.