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- UnratedDrug
Boehringer Ingelheim Pharmaceuticals, Inc. recalls Catapres (clonidine hydrochloride, USP) 0.1 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim
Boehringer Ingelheim recalls specific lots of Catapres 0.1 mg tablets after an extraneous peak was observed during dissolution testing.
Boehringer IngelheimOct 5, 2020 - Lower riskDrug
Med Shop Total Care Inc. recalls BUPIVACAINE HCL-BACLOFEN PF INJECTABLE 40MG-4000MCG/ML, 21 mL syringe, Rx only, Med Shop Total Care 470 East Loop 281
Med Shop Total Care recalls specific injectable anesthetic product due to non-sterility. Affected units contain lot #09282020@94. Consumers should contact the manufacturer for details.
Med Shop Total CareOct 5, 2020 - Lower riskFood
Bumble Bee Foods, LLC recalls Solid White Albacore Tuna in Water; Sold under brand names of Bumble Bee and Kirkland Signature: Bumble Bee NET WT 8-7
Bumble Bee Foods recalls solid white albacore tuna in water with swollen cans. Products sold under Bumble Bee and Kirkland Signature brands may be affected. Consumers should check UPC codes and use by dates.
Bumble BeeOct 5, 2020 - Lower riskFood
Meijer Inc./Traffic Dept. recalls FRESH FROM MEIJER FRUIT PALOOZA, 22oz Clear plastic container, UPC 220450514739
Meijer recalls 22oz clear plastic Fruit Palooza containers sold Sept 26-Oct 5, 2020 with potential Salmonella risk. Consumers should check UPC 220450514739 and contact Meijer for details.
MeijerOct 5, 2020 - Use cautionVehicle
FREIGHTLINER 108SD (2020) recall — Equipment
Daimler Trucks North America recalls 2020 Freightliner 108SD trucks with incorrect Gross Axle Weight Rating labels, risking vehicle overload and crashes. Owners must contact DTNA for free label updates.
Daimler Trucks North AmericaOct 4, 2020 - Use cautionVehicle
SPARTAN GLADIATOR (2020) recall — Parking Brake
Spartan is recalling 2019-2020 Gladiator and MetroStar Emergency vehicles due to potential park brake unintentional application causing loss of control. Owners must contact Spartan for free inspection and tightening.
SpartanOct 3, 2020 - Stop using nowVehicle
FORD TAURUS (2018) recall — Suspension
Ford recalls certain 2013-2018 Lincoln MKT, Ford Flex, and Taurus vehicles due to fractured rear suspension toe links that increase crash risk.
FordOct 2, 2020 - Use cautionVehicle
FOREST RIVER CEDAR CREEK (2020) recall — Equipment
Forest River recalls 2020 Cedar Creek trailers due to stove installed too close to window valance, risking fire. Owners must have valance replaced with non-combustible material and stove repositioned free of charge.
Forest RiverOct 2, 2020 - Use cautionDrug
Mylan Pharmaceuticals Inc. recalls Candesartan Cilexetil and Hydrochlorothiazide Tablets, USP 32 mg/12.5 mg, packaged in a) 90-count bottles (NDC
Mylan Pharmaceuticals recalls specific lots of Candesartan Cilexetil and Hydrochlorothiazide tablets due to out-of-specification organic impurities.
Mylan PharmaceuticalsOct 2, 2020 - Lower riskDrug
Medichem S.A. recalls Chlorhexidine Gluconate 20% 0012 Medichem, S.A. NDC 53296-0012-0
Medichem recalls specific batches of Chlorhexidine Gluconate 20% due to discoloration. Affected products may have visible color changes.
MedichemOct 2, 2020 - Stop using nowDrug
Marksans Pharma Limited recalls Time-Cap Labs, Inc. Metformin Hydrochloride Extended-Release Tablets USP 500 mg, a) 90 count (NDC 49483-623-09) b) 100
Marksans Pharma Limited recalls Time-Cap Metformin Hydrochloride Extended-Release Tablets (500mg) due to N-Nitrosodimethylamine (NDMA) impurity exceeding safe levels. Consumers should stop using affected batches.
Marksans Pharma LimitedOct 2, 2020 - Lower riskFood
Seneca Foods Corporation recalls Cinnamon Apple Crisps packaged under the following Brands and sizes: 1. Seneca, 2.5 ounce, UPC 0 18195-70100 8; 2.
Seneca Foods Corporation recalls cinnamon apple crisps due to possible Salmonella contamination. Affected products include Seneca and Clancy's brands with specific UPCs and dates. Consumers should check labels and contact Seneca for details.
SenecaOct 2, 2020 - Stop using nowFood
HU PRODUCTS recalls Primary/Retail Package labeled in part: "Hu; CHOCOLATE-COVERED HUNKS CASHEWS + VANILLA BEAN; VEGAN; ORGANIC; PALEO; Net
Hu Products recalls chocolate-covered cashews due to undeclared almonds. Check lot code 202183 and best-by date 05/21 for affected units.
Hu ProductsOct 2, 2020 - Lower riskMedical device
Medline Industries Inc recalls The Quidel Triage BNP Calibrators
Medline recalls Quidel Triage BNP Calibrators with shipment damage risks. Affected units include specific model numbers and expiration dates. Consumers should check their product details to determine if recalled.
MedlineOct 1, 2020 - UnratedMedical device
Microbiologics Inc recalls KWIK-STIK(TM), Streptococcus pneumoniae derived from ATCC(R) 49619(TM), packaged as follows: a. KWIK-STIK(TM) 2 Pack;
Microbiologics recalls KWIK-STIK products due to potential contamination with S. epidermidis, E. coli, and S. warneri. Affected units include 2-packs and 6-packs with specific catalog and lot numbers.
MicrobiologicsOct 1, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Conquest PTA Balloon dilation Catheter, 6mm x 40mm, 75 cm, Cat. No. CQ7564, UDI: (01) 00801741062902 - Product
Bard recalls Conquest PTA Balloon dilation Catheter (6mm x 40mm) due to incorrect balloon size. Using a smaller balloon may prolong procedures without serious injury risk.
BardOct 1, 2020 - Lower riskMedical device
Epitope Diagnostics, Inc. recalls EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of
Epitope Diagnostics recalls EDI Novel Coronavirus COVID-19 IgG ELISA Kit (KT-1032) due to potential reduced test accuracy from using deionized water instead of distilled water during manufacturing. Affected lots: P826, P815, P796, P776.
Epitope DiagnosticsOct 1, 2020 - Lower riskDrug
ASHTEL STUDIOS, INC. recalls Smart Care HAND SANITIZER, Ethyl Alcohol 62%, packaged in 0.84 FL.OZ (25 mL), labeled as a) Paw Patrol (Item #:
Ashtel Studios recalls Smart Care hand sanitizer with misleading food packaging. Products labeled as Paw Patrol, JoJo Siwa Dreamer, Hot Wheels, Barbie, Trolls, or Minions may resemble food pouches. Consumers should check labels for these specific designs.
Ashtel StudiosOct 1, 2020 - Lower riskFood
Desert Premium Group, LLC recalls Trader Joe's Hatch Valley Salsa, 12 oz. jars packed into trays of 12 and shrink-wrapped, UPC: 0053 6806, Dist. & Sold
Trader Joe's recalls Hatch Valley Salsa jars due to potential bacterial growth from a recorded pH of 6.65. Consumers should check UPC 0053 6806 for affected products.
Trader Joe'sOct 1, 2020 - Stop using nowFood
Country Fresh Inc. recalls Seasonal Trio 32oz UPC 681131180696 packaged in clear plastic container
Country Fresh recalls Seasonal Trio 32oz due to potential Listeria monocytogenes contamination. Check your clear plastic containers.
Country FreshOct 1, 2020 - Use cautionVehicle
ENTEGRA CORNERSTONE (2021) recall — Electrical System
Jayco is recalling 2021 Entegra Cornerstone motorhomes with potentially damaged power seat wiring that could cause fire. Owners should contact Jayco for free inspection and repair.
JaycoSep 30, 2020 - Use cautionVehicle
TESLA MODEL Y (2020) recall — Exterior Lighting
Tesla is recalling certain 2020 Model Y vehicles with a tow package that may not illuminate trailer brake lights during braking, increasing crash risk. Owners receive a free over-the-air software update.
TeslaSep 30, 2020 - Use cautionVehicle
BMW M5 (2020) recall — Back Over Prevention
BMW recalls 2020 M5 vehicles with potential rearview camera image obstruction, increasing crash risk. Owners must contact customer service for software update by November 18, 2020.
BMWSep 30, 2020 - Use cautionVehicle
BMW 530E (2020) recall — Electrical System
BMW recalls 2020 530E models due to debris in hybrid battery cells risking short circuits and fire. Owners must not charge or drive in manual/sport modes until repair.
BMWSep 30, 2020 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during
Maquet recalls BMU 40 blood monitoring units with model 701040852 due to insufficient PCB creepage distance (1.8mm vs required 4mm), potentially causing electrical issues during cardiac surgery.
MaquetSep 30, 2020 - UnratedMedical device
Merz North America, Inc. recalls COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns
Merz recalls COAPTITE Injectable Implant (model M0068903000) due to updated Instructions for Use not matching post-approval study data. Affected lots: 100127846-100129615.
MerzSep 30, 2020 - Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product Usage: For use in monitoring the performance of
Ortho Clinical Diagnostics recalls VITROS Anti-SARS-CoV-2 IgG Control products with elevated sample results risk. Affected units may show inaccurate test results; contact for remedy.
Ortho Clinical DiagnosticsSep 30, 2020 - Lower riskMedical device
XTANT Medical recalls XTANT Medical, ## mm x ## mm x # mm x # ,Lordotic/Packaged InTice - C, Sterile R, Single Use Only, for the following
XTANT Medical recalls cervical implants with incorrect titanium grade labels. Check product codes for CP Ti Grade 1-25 to avoid potential misidentification.
XTANT MedicalSep 30, 2020 - Stop using nowConsumer product

STIHL Recalls to Repair Mini-Cultivator Attachments Due to Laceration Hazard
STIHL recalls BF-KM Mini-Cultivator attachments with upside-down gearboxes that could cause lacerations if the tines rotate backward toward the user during operation.
STIHLSep 30, 2020 - Stop using nowConsumer product

Petzl Recalls Safety Ropes Due to Fall and Injury Hazard
Petzl recalls low-stretch kernmantle ropes with deep cuts or tape connecting ends that can fail, causing falls and injuries. Affected ropes have specific serial numbers and model numbers.
PetzlSep 30, 2020
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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.