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
Synthes (USA) Products LLC recalls DePuy Synthes 12.0MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic manual surgical instrument Part Code: 03.404.020S
DePuy Synthes recalls 12.0MM reamer heads for RIA 2 surgical use due to breakage risk when improper techniques are applied, potentially causing tissue damage.
DePuy SynthesNov 19, 2020 - UnratedDrug
Areva Pharmaceuticals Inc recalls Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 2 mL Single-Dose Vial, Rx Only, Distributed by: Areva
Areva Pharmaceuticals recalls 3,287 vials of Irinotecan Hydrochloride Injection due to CGMP deviations. Check lot numbers and expiration dates for affected units.
Areva PharmaceuticalsNov 19, 2020 - Lower riskDrug
US Pharmaceuticals Inc. recalls CVS Health Hydrating Healing Ointment (Petrolatum 41%), Net Wt 3 OZ (85g), Distributed by CVS Pharmacy, Inc. One CVS
US Pharmaceuticals recalls CVS Health Hydrating Healing Ointment (3 oz) with low weight fill tubes that may not meet quality standards. Consumers should check lot numbers and contact CVS for details.
US PharmaceuticalsNov 19, 2020 - Stop using nowConsumer product
Polaris Recalls RZR Recreational Off-Highway Vehicles Due to Injury Hazard (Recall Alert)
Polaris recalls 2020-2021 RZR models due to clutch failure hazard. Owners must stop using and get free repairs from dealers.
PolarisNov 19, 2020 - Use cautionVehicle
VOLKSWAGEN ATLAS (2021) recall — Back Over Prevention
Volkswagen recalls 2021 Atlas models with rear view camera issues causing black screens or freezes, increasing crash risk. Owners must update software free of charge by December 11, 2020 deadline.
VolkswagenNov 18, 2020 - Use cautionVehicle
KEYSTONE OUTBACK (2021) recall — Structure
Keystone is recalling certain 2019-2021 Outback 335CG and 340BH trailers due to potential frame rail buckling at the draw bar attachment point, which could increase crash risk.
KeystoneNov 18, 2020 - Use cautionMedical device
Aesculap Implant Systems LLC recalls ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Aesculap recalls ENNOVATE MIS REMOVALKEY SHORT (product code SZ380R) after risk of spinal fixation arm fracture during spinal surgery procedures.
Aescul: Aesculap Implant Systems LLCNov 18, 2020 - Use cautionMedical device
Becton Dickinson & Company recalls BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and
Becton Dickinson recalls BD PrecisionGlide 30G needles with blood contamination risk. If blood is not noticed before use, infection may occur. Affected units: Lot 9128897, expired June 2024.
Becton DickinsonNov 18, 2020 - Use cautionMedical device
Philips North America Llc recalls Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to
Philips recalls IntelliVue MP2 Patient Monitors (serial numbers DE73602213 and DE73602577) due to potential speaker failure that could delay critical patient treatment. Affected units may show 'Speaker Malfunct. INOP' or lack audible alarms.
PhilipsNov 18, 2020 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Optilite Freelite Mx Kappa Free Kit REF LK016.M.OPT.A
The Binding Site Group recalls Optilite Freelite Mx Kappa Free Kit REF LK016.M.OPT.A due to positive bias in quality control measurements. Affected units have specific model and lot numbers.
The Binding Site GroupNov 18, 2020 - Stop using nowMedical device
Shimadzu Medical Systems recalls MH-200S, system with Ceiling Suspended C-arm Support - Product Usage: intended to be used for cardiac angiography,
Shimadzu Medical Systems recalls MH-200S X-Ray systems with ceiling suspended C-arm support due to software causing ceiling arm movement after release. Affected serial numbers listed. Stop using immediately to prevent patient or operator injury.
Shimadzu Medical SystemsNov 18, 2020 - Use cautionMedical device
Boston Scientific Corporation recalls IceSeed" 1.5 Cryoablation Needle
Boston Scientific recalls IceSeed 1.5 Cryoablation Needles with reported gas leaks. Affected units have specific batch numbers and UDIs. Stop using immediately to prevent potential injury.
Boston ScientificNov 18, 2020 - UnratedDrug
The Harvard Drug Group recalls Aripiprazole Tablets, USP, 15 mg, 30 tablets per unit dose carton, Rx Only, Manufactured by: Apotex, Inc, Toronto,
Harvard Drug Group recalls 15mg Aripiprazole tablets with failed dissolution specs. Affected lots T02520 and T02637 expired 02/2021. No remedy stated in recall notice.
The Harvard Drug GroupNov 18, 2020 - UnratedDrug
Fusion Health and Vitality LLC recalls Immune Boost with natural strawberry flavor, 8,000 IU, Supports a Healthy and Balanced Immune System, 60 mL bottle,
Fusion Health recalls Immune Boost with natural strawberry flavor due to being marketed with drug claims without FDA approval. Consumers should check lot numbers 200407-200608 for affected products.
Fusion HealthNov 18, 2020 - Stop using nowFood
Hong Thai Foods Corp recalls Golden Boy brand Custard muffin Pandan 7.76 ounce, rigid clear plastic packages
Hong Thai Foods Corp recalls Golden Boy brand Custard muffin Pandan (7.76 oz) due to undeclared milk. Check your Best Before date and UPC.
Golden BoyNov 18, 2020 - Use cautionVehicle
VOLKSWAGEN ATLAS CROSS SPORT (2020) recall — Steering
Volkswagen is recalling 2020-2021 Atlas Cross Sport vehicles with potentially damaged steering knuckles that could cause loss of steering and increase crash risk. Owners must have vehicle inspected by dealer.
VolkswagenNov 17, 2020 - Stop using nowVehicle
THOR MOTOR COACH FREEDOM ELITE (2020) recall — Electrical System
Thor recalls certain 2020-2021 motorhomes due to water entering the electrical system, creating a fire risk. Dealers will replace the part free of charge.
Thor Motor CoachNov 17, 2020 - Use cautionVehicle
TESLA MODEL Y (2020) recall — Suspension
Tesla is recalling certain 2020 Model Y vehicles due to potential detachment of the front upper control arm, which could decrease steering ability and increase crash risk. Owners should contact Tesla for free inspection and tightening.
TeslaNov 17, 2020 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
Zimmer Biomet recalls Polaris 5.5 Spinal Systems due to risk of spinal screw failure when used with direct current stimulation systems. Affected items include specific model numbers and kits sold in the US.
Zimmer BiometNov 17, 2020 - Use cautionMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended
Recall of Tempus LS manual defibrillators with software version 1.3.4 due to potential delay in therapy when switching between pacer and manual modes. Affected units have specific serial numbers.
Remote Diagnostic TechnologiesNov 17, 2020 - Use cautionMedical device
Boston Scientific Corporation recalls Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF
Boston Scientific recalls Lotus Edge Valve System (23mm) due to risk of deployment failure if visual inspection is skipped during valve locking. Affected units have specific lot numbers and expiration dates.
Boston ScientificNov 17, 2020 - Lower riskDrug
Fresenius Kabi USA, LLC recalls Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL Single Dose Bottle, Rx only,
Fresenius Kabi recalls specific dexmedetomidine injection due to trace lidocaine contamination. Patients using this medication may face unintended effects from cross-contamination.
Fresenius KabiNov 17, 2020 - Stop using nowDrug
MPM Medical LLC recalls REGENECARE HA (Lidocaine HCL 2%) Topical Anesthetic Hydrogel, Net Wt. 3 oz. (85 g), Manufactured For: MPM Medical
MPM Medical recalls lidocaine hydrogel products contaminated with Burkholderia cepecia bacteria. Consumers should stop using affected items to avoid infection risks.
MPM MedicalNov 17, 2020 - UnratedDrug
BASF Corporation recalls Kollidon CL-M Crospovidone Ph.Eur.Type B, USP/NF, JP, micronized, packaged in 30 kg plastic drums, Manufacturer: BASF
BASF recalls Kollidon CL-M Crospovidone Ph.Eur.Type B, USP/NF, JP, micronized in 30kg plastic drums due to cross contamination with theophylline. This may pose health risks if used in medications.
BASFNov 17, 2020 - Lower riskDrug
Golden State Medical Supply Inc. recalls ARIPIPRAZOLE TABLETS, 15 mg, 30-count. bottles, Rx Only, GSMS Incorporated, Manufactured by: Apotex Inc. Toronto,
Golden State Medical Supply recalls 15mg Aripiprazole tablets due to possible out-of-spec dissolution. Check NDC #60429-449-30 and lot numbers for affected products.
Golden State Medical SupplyNov 17, 2020 - Lower riskDrug
Fresenius Kabi USA, LLC recalls DOXOrubicin Hydrochloride Injection, USP, 10 mg / 5 mL (2 mg / mL), 5 mL fill in a 6 mL vial, Single Dose Vial, Rx
Fresenius Kabi recalls DOXOrubicin Hydrochloride Injection due to trace octreotide contamination. This may cause cross-contamination with other products. Affected units have NDC 63323-883-05, batch 6120525.
Fresenius KabiNov 17, 2020 - UnratedDrug
Taro Pharmaceuticals U.S.A., Inc. recalls Kroger Athlete's Foot Cream, Clotrimazole Cream USP, 1%, Antifungal, NET WT 0.5 OZ (15g), Distributed by The Kroger Co.
Taro Pharmaceuticals recalls Kroger Athlete's Foot Cream due to undetected impurities in Clotrimazole Cream USP 1%. Affected products have specific lot numbers and expiration dates. Consumers should check labels and contact Kroger for details.
Taro PharmaceuticalsNov 17, 2020 - Lower riskFood
Fusion Health and Vitality LLC recalls PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g)
Fusion Health is recalling PHARMORIGINS CORE supplements because they contain an unapproved food additive and marketing claims. Stop using if you have the product with specific lot numbers.
Fusion HealthNov 17, 2020 - Stop using nowFood
Victoria Gourmet, Inc. recalls Victoria Taylor Seasonings Sicilian Seasoning/Assaisonement Sicilien; Italian style seasoning blend; 2.5oz; packaged in
Victoria Gourmet recalls 1,080 jars of Sicilian Seasoning due to undeclared sesame. Check your pantry if you bought this Canadian product.
Victoria Taylor SeasoningsNov 17, 2020 - Use cautionVehicle
FLEETWOOD DISCOVERY (2021) recall — Equipment
REV is recalling 2021 Fleetwood Discovery motorhomes due to a bed frame drop risk. The bed lift motor may fail, causing the bed to drop. Owners should contact REV customer service for free replacement.
REVNov 16, 2020
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