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
35,004 found- Lower riskMedical device
Cuattro LLC recalls CuattroDR System Software, REF: SWR-00069-MD, UDI: B269SWR00069MD0
Cuattro LLC recalls software version 4.4.128 due to potential misdiagnosis from showing previous patient images in later studies. Affected units have specific reference and UDI codes.
CuattroOct 15, 2019 - Stop using nowDrug
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item:
Viatrexx recalls Viatrexx-Hair 10 mL vials due to sterility concerns. Check lot numbers and expiration dates for affected products distributed to physicians.
ViatrexxOct 15, 2019 - Stop using nowFood
Citrus World, Inc. recalls Disney Donald Duck Kiwi Strawberry Flavored Four Juice Cocktail 20 OZ
Citrus World, Inc. recalls Disney Donald Duck Kiwi Strawberry Flavored Four Juice Cocktail 20 OZ due to potential mold contamination.
Citrus WorldOct 15, 2019 - Lower riskFood
ALFA INTERNATIONAL SEAFOOD INC recalls Full Moon Fish Tuna Steaks, Skinless, Boneless, IVP, Size: 8 oz, Net Weight 5 lbs
ALFA International Seafood recalls 8oz tuna steaks with wrong production and expiry dates on labels. Consumers should check labels for incorrect manufacturer numbers, pack dates, and expiration dates.
ALFA International SeafoodOct 15, 2019 - Lower riskFood
Peekay International, Inc. recalls Bulk Dry Apricot in clear plastic bags inside brown cardboard box and Swan brand Dry Appricot & Keshav brand Dry
Peekay International recalls bulk dry apricots with undeclared sulfites. Consumers should check UPCs for affected products and contact the company for details.
PeekayOct 15, 2019 - Use cautionMeat & poultry
Kenosha Beef International Recalls Seasoned Beef Products due to Possible Foreign Matter Contamination
Kenosha Beef International recalls seasoned beef products from Sept 20 to Oct 4, 2019, due to possible metal shavings contamination. Products should be thrown away or returned to the place of purchase.
Kenosha Beef InternationalOct 14, 2019 - Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls Urine Electrolyte Diluent, Product Code: 1112352 - Product Usage: used to dilute urine specimens for analysis of sodium
Ortho Clinical Diagnostics recalls Urine Electrolyte Diluent (Product Code 1112352) due to potential instability when stored in 2mL cups for 7 days. Affected lots have expiry dates from Feb 2020 to Aug 2021.
Ortho Clinical DiagnosticsOct 14, 2019 - Use cautionMedical device
Mizuho OSI recalls Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI -
Mizuho OSI recalls Levo Arm Label models 7887-050 and 7887-050R due to potential fluid ingress causing electrical failure and locking mechanism issues during spinal surgery. Affected units have serial numbers listed in the recall notice.
Mizuho OSIOct 14, 2019 - Use cautionMedical device
Becton Dickinson & Company recalls BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)
Becton Dickinson recalls Canadian BD Posiflush Pre-Filled Normal Saline Syringes (Catalog 306575) due to risk of mixing with non-human-use syringes. Affected units have specific labels and lot numbers.
Becton DickinsonOct 14, 2019 - Lower riskMedical device
Abbott Medical recalls Radiofrequency Grounding Pad, REF RF-DGP-L
Abbott Medical recalls Radiofrequency Grounding Pads with incorrect release liner orientation that may cause uneven heating during use. Affected units have specific batch numbers and UDI codes.
Abbott MedicalOct 14, 2019 - Stop using nowFood
Vita Food Products, Inc. recalls NATHAN'S COLD SMOKED WILD SALMON, in 3oz.vacuum packed pouch, 12 units per wholesale case, UPC 73030 80686
Vita Food Products recalls Nathan's Cold Smoked Wild Salmon due to Listeria monocytogenes. Check lot codes and UPC before consuming.
Nathan'sOct 14, 2019 - Stop using nowFood
Samurai, Inc. recalls Samurai Brand Furikake Popcorn Net Wt. 5 oz. (142g), foil bag - sold by single bag or case of 20 Made in Hawaii BAG
Samurai, Inc. recalls Furikake Popcorn due to undeclared fish allergen. Check your bags for specific Best By dates and UPCs.
SamuraiOct 14, 2019 - Lower riskFood
Vitamin Cottage Natural Foods Market, Inc DBA Natural Grocers recalls Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin
Natural Grocers recalls organic soybeans in 2lb plastic bags due to potential mold contamination. Consumers should check product codes and stop using if mold is present.
Natural GrocersOct 14, 2019 - Use cautionVehicle
KEYSTONE SPRINGDALE (2020) recall — Equipment
Keystone is recalling certain 2020 Springdale trailers due to incorrect tire labels that may cause overinflation, affecting stability and increasing crash risk. Owners must return for free replacement Federal Identification Tags.
KeystoneOct 12, 2019 - Lower riskMeat & poultry
YOUBITE, LLC Recalls Pork Sausage and Turkey Sausage Products due to Mislabeling
USDA recalls 7,197 pounds of YOUBITE pork and turkey sausages with unlisted casings due to mislabeling. Consumers urged not to eat these products.
YOUBITEOct 11, 2019 - Lower riskMedical device
TELEFLEX MEDICAL INC recalls Sprotte Needle, REF 32115130C w/ Intro 22 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needles
Teleflex Medical recalls Sprotte lumbar puncture needles with specific batch numbers due to potential packaging issues that may compromise sterility. Affected users should contact Teleflex for details.
Teleflex MedicalOct 11, 2019 - Stop using nowMedical device
Stryker Communications recalls Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000
Stryker recalls Berchtold Chromophare ceiling-mounted surgical lights with catalog #CH13000000 due to risk of falling, potentially causing serious injury to patients or healthcare providers.
StrykerOct 11, 2019 - Lower riskMedical device
AMD Medicom Inc. recalls MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040
Medicom recalls Level :2 masks (Item 2040) that may be in Level 3 boxes. Using these masks risks lower protection than intended. Affected masks were sold with Lot 1917.
MedicomOct 11, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH 930 Analyzer, Siemens Material Number 11067000, Software Versions V1.19.2 or 1.20.0 The Atellica CH 930
Siemens recalls Atellica CH 930 analyzers with software versions V1.19.2 or 1.20.0 that may display incorrect test results when scanning barcodes for certain fluids due to decimal point translation.
Siemens HealthcareOct 11, 2019 - Lower riskMedical device
Nucryo Vascular Inc. recalls The PolarCath Balloon Catheter consists of a coaxial catheter shaft with two concentric, non-compliant balloon systems
Nucryo Vascular recalls specific PolarCath Balloon Catheter lots due to mislabeled sterilization. E-Beam sterilized units labeled as EO sterilized may pose risks. Affected lots include CAT 0738-0758.
Nucryo VascularOct 11, 2019 - Lower riskMedical device
Implant Direct Sybron Manufacturing LLC recalls Implant Direct, CE 0086, REF: 855710, Legacy 3 Impant, Surface: SBM, Qty:1, Size:5.7mmD x 10mmL, 5.7mmD Platform,
Implant Direct recalls Legacy 3 implants with incorrect cover screw that may delay surgery or require new procedures. Affected units have specific size and lot numbers.
Implant DirectOct 11, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Giraffe Incubator Carestation, Giraffe Incubator Carestation CS1 infant warmer
GE Healthcare recalls Giraffe Incubator Carestation CS1 infant warmers due to potential patient falls from unsecured panels. Affected units include all model numbers with specific identifiers.
GE HealthcareOct 11, 2019 - Lower riskMedical device
LIFELINES NEURO COMPANY recalls ElectroTek Temporal Sensor Cable Gold - Long Length, Graduated - Product Usage: The electroencephalographic system
Lifelines Neuro recalls ElectroTek Temporal Sensor Cable Gold for potential incorrect electrode labels that could lead to EEG study errors. Affected units have specific model and lot codes.
Lifelines NeuroOct 11, 2019 - Lower riskMedical device
Medtronic Neuromodulation recalls Synchromed II programmable pump, Model numbers 8637-20 and 8637-40
Medtronic recalls Synchromed II programmable pumps with model numbers 8637-20 and 8637-40 due to potential foreign particles in the motor assembly that could cause motor stalls. Affected units have specific serial numbers listed in the recall notice.
Medtronic NeuromodulationOct 11, 2019 - Use cautionDrug
X-Gen Pharmaceuticals Inc. recalls Levetiracetam Injection, 500 mg/5mL, 10 single-use 5 mL vials, Rx only, Manufactured by: Agile Specialties Private
X-Gen Pharmaceuticals recalls Levetiracetam Injection vials due to incorrect package inserts. Check lot numbers and expiration dates for affected units.
X-Gen PharmaceuticalsOct 11, 2019 - Stop using nowFood
Relish Foods, Inc. dba Gourmet Fusion Foods, Inc. recalls Trade Winds Premium Grade Yellowfin (Ahi) Tuna Ground Keep Frozen Net Weight 10 LBS. (4.54 KG) Product of Vietnam
Relish Foods recalls Trade Winds Premium Grade Yellowfin Tuna Ground due to elevated histamine levels. Check your freezer for affected lots immediately.
Trade WindsOct 11, 2019 - Lower riskFood
Great Lakes Cheese Co Inc recalls Pasteurized Process American Cheese, yellow, 6 - 5lb loaves per case. Brands as follows: 1) Wegmans; 2) Market Basket;
Great Lakes Cheese Co recalls yellow Pasteurized Process American cheese (6-5lb loaves) sold by Wegmans, Market Basket, Cabot, Field, Foodtown, and Hannaford due to potential metal foreign material. Consumers should check expiration dates and contact the manufacturer for details.
Great Lakes Cheese CoOct 11, 2019 - Use cautionVehicle
HONDA RIDGELINE (2014) recall — Vehicle Speed Control
Dorman recalls accelerator pedals for 2014 Honda Ridgeline models that may bind, causing engine to not return to idle quickly and increasing crash risk. Owners must contact Dorman for free replacement.
DormanOct 10, 2019 - Use cautionVehicle
TESLA MODEL 3 (2019) recall — Equipment
Tesla is recalling 2019 Model 3 vehicles with driver-side sun visors that lack required airbag warning information, failing FMVSS 208. Owners must have visors inspected and replaced free by Tesla.
TeslaOct 10, 2019 - Stop using nowVehicle
FORD RANGER (2019) recall — Visibility
Ford recalls certain 2019 Rangers due to an electrical short in the HVAC blower motor that increases fire risk. Check if your vehicle is affected.
FordOct 10, 2019
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83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.