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
35,006 found- Lower riskMedical device
Medtronic Navigation, Inc. recalls StealthStation" S7 System with Polaris Spectra Camera part number PSU 9733437 - Product Usage: are intended as an aid
Medtronic recalls StealthStation S7 System with Polaris Spectra Camera (PSU 9733437) due to potential navigation inaccuracies of 6mm when using both active and passive trackers simultaneously. No injuries reported.
MedtronicJun 5, 2020 - Lower riskMedical device
OrthoPediatrics Corp recalls OrthoPediatrics ACL Reconstruction System ShieldLoc 7mm implant component model number 10-1008-4070 - Product Usage: is
OrthoPediatrics recalls ACL Reconstruction System ShieldLoc 7mm implant components with incorrect size labels. Products labeled 10-1008-4070 may contain 10-1008-4060, and vice versa. This could lead to improper surgical fixation.
OrthoPediatricsJun 5, 2020 - Lower riskDrug
PD-Rx Pharmaceuticals, Inc. recalls metFORMIN HCL ER 500 mg, a) 30 tablets (NDC 72789-009-30); b) 60 tablets (NDC 72789-009-60); c) 90 tablets (NDC
PD-Rx Pharmaceuticals recalls metformin ER 500mg tablets with N-Nitrosodimethylamine (NDMA) impurity above safe levels. Consumers should stop using affected lots.
PD-RxJun 5, 2020 - Lower riskDrug
PD-Rx Pharmaceuticals, Inc. recalls metFORMIN HCL ER USP 500 mg, a) 30 tablets (NDC: 43063-428-30); b) 60 tablets (NDC: 43063-428-60); c) 90 tablets (NDC:
PD-Rx Pharmaceuticals recalls metformin ER 500mg tablets with N-Nitrosodimethylamine (NDMA) impurity above safe levels. Consumers should stop using affected lots.
PD-RxJun 5, 2020 - UnratedDrug
Akorn, Inc. recalls Prednisolone Sodium Phosphate Oral Solution, 5 mg/5 mL, 120 mL Bottle, Rx only, HI-TECH PHARMACAL CO., INC.,
Akorn recalls 17,424 bottles of Prednisolone Sodium Phosphate Oral Solution due to discoloration. Check lot numbers 365566 and 365568.
AkornJun 5, 2020 - Use cautionDrug
Marksans Pharma Limited recalls Time-Cap Labs, Inc. Metformin Hydrochloride Extended-Release Tablets, USP 500 mg Rx Only 100 Tablets bottles,
Time-Cap Labs recalls 500 mg Metformin ER tablets due to N-Nitrosodimethylamine (NDMA) impurity above acceptable levels. Check your bottle.
Time-Cap LabsJun 5, 2020 - Lower riskFood
Stumptown Coffee Corp recalls Stumptown Cold Brew Coffee and Chocolate with Oatmilk. Product is TetraPak Prisma Pak aseptic packaging. Keep
Stumptown Coffee Corp recalls Cold Brew Coffee and Chocolate with Oatmilk due to packaging leakage. Products were made in late October 2020 and may leak if stored improperly.
Stumptown CoffeeJun 5, 2020 - Use cautionVehicle
KTM 790 ADVENTURE (2020) recall — Service Brakes, Hydraulic
KTM recalls 2019-2020 790 Adventure motorcycles due to rear brake hose overheating that can cause brake system failure and crash risk. Owners must contact KTM for free brake line repair.
KTMJun 4, 2020 - Use cautionVehicle
KENWORTH T680 (2020) recall — Electronic Stability Control (Esc)
PACCAR recalls 2020 Kenworth T680 trucks with NAMUX software that may not warn drivers if ABS loses power, risking crashes. Owners must update software free via dealer.
KenworthJun 4, 2020 - Lower riskMedical device
HF Acquisition Co., LLC recalls STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing various products to include Narcan Nasal spray,
HF Acquisition recalls STAT KIT Model 550AI Emergency Medical Kits with 1 dose of Narcan Nasal spray instead of 2. This may cause insufficient overdose treatment.
HF AcquisitionJun 4, 2020 - Use cautionMedical device
Cardinal Health 200, LLC recalls Cardinal Health NPWT Canister with Gel 300cc, Prescription Only - Product Usage: The systems are intended for use on
Cardinal Health recalls NPWT Canister with Gel 300cc (model 47-4000) due to potential oversized O-ring causing installation failure. Prescription-only device for wound care.
Cardinal HealthJun 4, 2020 - Lower riskMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Percepta CRT-P MRI, Model Numbers: a) W1TR01, b) W1TR04, c) W4TR01, d) W4TR04
Medtronic recalls Percepta CRT-P MRI devices with specific model numbers due to a rare temporary suspension of device features during certain device interrogations. Features automatically resume after next interrogation or magnet presence. No patient impact expected.
MedtronicJun 4, 2020 - UnratedMedical device
Boston Scientific Corporation recalls Ablation Galil Technology, IcePearl¿2.1 CX Prostate¿Kit Visual Ice System, Prescription Only Galil Medicals 2.1 CX
Boston Scientific recalls IcePearl 2.1 CX Prostate Kit Visual Ice System for potential needle surface deterioration during procedures. Affected units include specific batch numbers and model codes. Contact for remedy details.
Boston ScientificJun 4, 2020 - Lower riskDrug
AVKARE Inc. recalls Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, a) 50 count (NDC 50268-531-15); b) 90 count (NDC
AVKARE recalls Metformin Hydrochloride Extended-Release Tablets 500mg with N-Nitrosodimethylamine (NDMA) impurity above acceptable levels. FDA analysis detected this impurity in specific batch numbers and expiration dates.
AVKAREJun 4, 2020 - Lower riskDrug
SOMERSET THERAPEUTICS LLC recalls Brimonidine Tartrate Opthalmic Solution 0.2%, 10 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC
SomerSET Therapeutics recalls Brimonidine Tartrate Ophthalmic Solution 0.2% 10mL bottles (Rx only) manufactured in India with specific lot numbers due to slow leaching from product label affecting product quality over time.
SomerSET TherapeuticsJun 4, 2020 - Use cautionConsumer product
Tim Trading Recalls Emori Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Tim Trading recalls Emori Wintergreen Essential Oil due to non-child-resistant packaging, posing poisoning risk for young children. Consumers should store out of reach and contact for refund or replacement.
EmoriJun 4, 2020 - Use cautionConsumer product
Capstone Holdings Recalls Simply Earth Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Simply Earth recalls Wintergreen Essential Oil due to non-child-resistant packaging, posing poisoning risk to young children. Consumers should store out of reach and get free replacement.
Simply EarthJun 4, 2020 - Stop using nowVehicle
VOLKSWAGEN ARTEON (2019) recall — Service Brakes
Volkswagen is recalling 2019 Arteons due to a potentially disconnected brake input rod. Dealers will inspect and repair the issue free of charge starting April 3, 2020.
VolkswagenJun 3, 2020 - Use cautionVehicle
TRIPLE E RV WONDER (2020) recall — Electrical System
Triple E is recalling 2020 Wonder travel trailers due to unsecured ceiling light wiring that can arc and cause fire. Owners should contact customer service for free repairs.
Triple EJun 3, 2020 - Use cautionVehicle
ARCIMOTO FUV (2020) recall — Electrical System
Arcimoto is recalling 2019-2020 FUV motorcycles with improperly crimped traction-power harnesses that could cause crashes or fires. Owners must contact customer service for free replacement.
ArcimotoJun 3, 2020 - Lower riskMedical device
Roche Molecular Systems, Inc. recalls MagNA Pure 96 Instrument, clinical sample concentrator, Material number 06541089001 - Product Usage: This protocol is
Roche recalls MagNA Pure 96 clinical sample concentrators used with Sample Transfer protocol 3.0 due to cross-contamination risk. Affected units may cause erroneous lab results.
RocheJun 3, 2020 - Use cautionMedical device
LONGHORN VACCINES AND DIAGNOSTIC recalls PrimeStore Molecular Transport Medium (PS-MTM), Model Numbers LH-1-2, LH-1-3, LH-1-4, LH-1-5, LH-1-5CC, LH-1-15CC -
Longhorn Vaccines and Diagnostic recalls PS-MTM tubes (models LH-1-2 to LH-1-15CC) that may lack labels. Without labels, users can't identify tubes, and if samples are tested with bleach-containing reagents, cyanide gas may form. Affected lab users should check labels and avoid using unlabeled tubes.
Longhorn Vaccines and DiagnosticJun 3, 2020 - Stop using nowMedical device
Dufner Instrumente GmbH recalls DUFNER Instrumente GmbH-De Bakey Slim Needleholder- intended to hold a suturing needle for closing wounds during
Dufner recalls slim needleholders with lot numbers 8170368 and 81806: Tungsten carbide plate may break under pressure, causing tissue injury during surgery.
DufnerJun 3, 2020 - Lower riskMedical device
Coltene Whaledent Inc recalls HYGENIC Wingless Fiesta Kit, Model no. H02790 - Product Usage: The dental dam forceps are intended to be used in
Coltene recalls HYGENIC Wingless Fiesta Kit (Model H02790) with batch numbers 1903-1940 due to forceps that may not fit dental dam clamps properly. Affected users should check batch numbers and return if issues occur.
ColteneJun 3, 2020 - Lower riskMedical device
CooperSurgical, Inc. recalls COOPERSURGICAL Os FinderTM Cervical Dilator, Taper: 2.0 mm to 4.0 mm OD Length: 21.5 cm Box of 50 Part Number: 1176
CooperSurgical recalls Os Finder Cervical Dilators (Part 1176) due to mislabeling. Products may show incorrect part numbers on packaging. Consumers should check labels and contact the company for details.
CooperSurgicalJun 3, 2020 - Lower riskDrug
A.P. Deauville, LLC recalls Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc), 14.4 FL OZ. (426 mL), A.P. Deauville LLC New Brunswick,
Powerstick recalls Soft Whisper Dandruff Shampoo due to water quality failing USP specifications. Affected lots from 070421E211 to 071021E241, expiring 7/2: stop using and contact for details.
PowerstickJun 3, 2020 - Stop using nowDrug
Yusef Manufacturing Laboratories, LLC recalls Rocky Mountain Sunscreen SPF30 Kiwi Flavored Lip Balm (Oxybenzone 5%, Meradimate 5%, Octinoxate 7.5%, Octisalate 5%)
Rocky Mountain Sunscreen recalls SPF30 Kiwi Flavored Lip Balm due to excessive Octisalate (15% above label). Consumers should check product details and contact the manufacturer for guidance.
Rocky Mountain SunscreenJun 3, 2020 - UnratedDrug
WALKER EMULSIONS INC recalls Walker Emulsions Hand Sanitizer (60%), Non-Sterile Solution, Alcohol Antiseptic 60%, 1 Gallon, Topical Solution, Walker
Walker Emulsions recalls 1-gallon hand sanitizer due to unapproved ethanol content. Consumers should check NDC 74940-0415-1 and lot #209638 for affected products.
Walker EmulsionsJun 3, 2020 - Lower riskFood
Toufayan Bakery, Inc. recalls TOUFAYAN BAKERIES SMART POCKETS EVERYTHING 6 COUNT NET WT 7.4 OZ. (210 g), UPC 0 7312400792 7. 12 packages per case.
Toufayan Bakery recalls 12-packs of Smart Pockets Everything 6-count bags due to undeclared sesame, poppy seeds, and dehydrated garlic. Consumers should check product dates and contact the company for details.
Toufayan BakeryJun 3, 2020 - Use cautionVehicle
MAZDA CX-5 (2016) recall — Exterior Lighting
Mazda recalls 2016 CX-5 vehicles with potential DRL failure causing reduced visibility and crash risk. Owners must have headlights inspected and repaired free by dealers.
MazdaJun 2, 2020
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