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
34,959 found- Lower riskMedical device
Edwards Lifesciences, LLC recalls Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a 10.5 Fr (3.5mm), triple lumen, 100cm long
Edwards Lifesciences recalls a limited number of IntraClude intra-aortic occlusion devices due to potential inter-lumen leaks between cardioplegia and pressure lumens, which could affect medical procedures.
Edwards LifesciencesJan 16, 2019 - Lower riskMedical device
Polymer Technology Systems, Inc. recalls CHOL+HDL+GLU test strips, REF 2412
Polymer Technology Systems recalls CHOL+HDL+GLU test strips REF 2412 due to potential incorrect results from test strips falling out during analysis. Affected lots include I808, I809, I811, I812, I814.
Polymer Technology SystemsJan 16, 2019 - UnratedMedical device
Carolina Liquid Chemistries recalls CAROLINA(R) LIQUID CHEMISTRIES CORP. ETHA RGT. KIT, IVD, REF ST321
Carolina Liquid Chemistries recalls Etha Rgt Kit IVD Ref ST321 due to potential safety concerns. Affected units include Lot 11686.
Carolina Liquid ChemistriesJan 16, 2019 - Lower riskDrug
KRS Global Biotechnology, Inc recalls NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF), 16 mg / 250 mL, 250 mL IV bag, Rx only, KRS Global
KRS Global recalls NORepinephrine 16 mg IV bags with labeling mix-up. This affects specific lot numbers and may cause confusion in medical use. Contact for details.
KRS GlobalJan 16, 2019 - Lower riskDrug
Rx Pak Division of McKesson Corporation recalls Docusate Sodium, 100mg softgels, packaged in 10 x 10 unit dose blister cards, For institutional use only, Mfg by:
Rx Pak recalls Docusate Sodium 100mg softgels due to label mix-up with Gabapentin 300mg. Institutional users should check packaging for correct labeling to avoid confusion.
Rx PakJan 16, 2019 - Stop using nowFood
Puratos Corporation recalls Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.
Puratos Corporation recalls 25,700 lbs of Tegral Satin Gold CL Crème Cake because it contains undeclared milk. Check your product details.
PuratosJan 16, 2019 - Use cautionFood
Ventura Foods Llc recalls Sysco Classic Liquid Margarine; 2 x 17.5 lb. plastic containers; 99961WFS
Ventura Foods recalls Sysco Classic Liquid Margarine due to mislabeled packaging that fails to declare soy lecithin, posing an allergy risk.
Sysco ClassicJan 16, 2019 - Stop using nowVehicle
JEEP WRANGLER (2016) recall — Air Bags
Chrysler recalls 2016 Jeep Wrangler models with a risk of air bag inflator explosion during crashes, potentially causing serious injury or death. Owners must stop driving until repair is complete.
ChryslerJan 15, 2019 - Use cautionMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or
Fujifilm recalls FDR Go PLUS mobile X-ray systems with serial numbers MQ0001281001 to MQ00012: The braking mechanism may not engage when the handle is released, potentially causing unintended movement during use.
Fujifilm Medical SystemsJan 15, 2019 - Lower riskMedical device
Miami Device Solutions, LLC. recalls Proximal Humerus Plate, 8 holes, Right, REF MDS130108R - Product Usage: The Proximal Humerus Plating System consists of
Miami Device Solutions recalls right-sided Proximal Humerus Plates (REF MDS130108R) due to risk of improper identification as left side. This affects orthopedic implants used in fracture repairs.
Miami Device SolutionsJan 15, 2019 - Lower riskMedical device
Westmed, Inc. recalls Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask; Circuit for use on compatible Infant Resuscitators.
Westmed recalls Neo-Vent Infant T-Piece Resuscitation Circuits with 15mm OD connections that may not fit infant resuscitators. Affected units have specific model numbers and were sold in 2018.
WestmedJan 15, 2019 - Stop using nowDrug
Dr. Reddy's Laboratories, Inc. recalls Ezetimibe and Simvastatin Tablets 10mg/80 mg, 1000-count bottles, Rx only, Manufactured by: Teva Pharmaceuticals Ind.
Dr. Reddy's recalls 1000-count Ezetimibe and Simvastatin tablets with black speckles. Consumers should check NDC 43598-586-10 and lot numbers 43E021/43E023 for affected products.
Dr. Reddy'sJan 15, 2019 - Lower riskDrug
Advanced Pharma Inc. recalls HEPERAIN 50 mg/50 mL (1mg/mL) Injectable Solution, Heparin Sodium 0.45% Sodium Chloride QS Heparin 50 Units 50 mL,
Advanced Pharma recalls Heparin injectable solution due to label error stating 50 mg/50 mL instead of 50 Units/50 mL. This could lead to incorrect dosing. Check your product's NDC 42852-725-65 and lot 12/19/18 0242 72565S.
Advanced PharmaJan 15, 2019 - Use cautionDrug
LUPIN SOMERSET recalls Fluocinolone Acetonide Topical Solution, USP, 0.01 %, 60 mL bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals,
Lupin Pharmaceuticals recalls 24,180 bottles of Fluocinolone Acetonide Topical Solution due to elevated impurities from oxidative degradation.
Lupin SomersetJan 15, 2019 - Use cautionDrug
Tris Pharma Inc. recalls infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 1 FL
Tris Pharma recalls infant ibuprofen oral suspension with possible higher concentration than labeled. Consumers should check product details and contact the company for guidance.
Tris PharmaJan 15, 2019 - Stop using nowFood
Ottogi America Inc recalls Ottogi Ppushu Ppushu BBQ Flavor 3.17oz x 40ea Item #21503007 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by:
Ottogi America Inc. recalls Ppushu Ppushu BBQ Flavor snacks due to undeclared egg allergen. Check your package for the best before date range.
OttogiJan 15, 2019 - Stop using nowVehicle
BMW X5 (2011) recall — Air Bags
BMW is recalling certain 2011 X5 models due to passenger air bag inflators that may explode in crashes, causing serious injury or death. Owners must stop driving until fixed.
BMWJan 14, 2019 - Use cautionVehicle
VOLVO VNL (2019) recall — Power Train
Volvo recalls 2018-2019 VNL trucks with automated manual transmission due to potential unintended vehicle movement causing crashes.
VolvoJan 14, 2019 - Use cautionVehicle
LINCOLN NAUTILUS (2019) recall — Lane Departure
Ford recalls 2019 Lincoln Nautilus vehicles with Lane Center Assist system that may not detect driver hands on wheel, increasing crash risk. Owners must update software free via dealer.
FordJan 14, 2019 - Use cautionMedical device
Shimadzu Medical Systems Usa Com recalls SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to
Shimadzu Medical Systems recalls MX8 Mobile X-Ray systems that may continue moving if operator releases handle without braking. Affected units have serial numbers starting with 41F41DD7C001 to 41F41DD85004. No remedy provided.
Shimadzu Medical SystemsJan 14, 2019 - Use cautionMedical device
3M Company - Health Care Business recalls 3M(TM) Surgical Clipper by Remington(R) REF 9602 The 3M Surgical Clipper Classic, 9602, is intended to remove body hair
3M recalls its Surgical Clipper Classic model 9602 for overheating when charged with modified sine wave inverters. This could cause fire or injury during emergency medical use.
3MJan 14, 2019 - Lower riskMedical device
Teleflex Medical recalls RUSCH Urinary Drainage bag, 2000mlm REF 390060 urine collection device
Teleflex Medical recalls RUSCH 2000ml urinary drainage bags with non-compliant UDI labels. The missing UDI information does not affect device function but may cause regulatory issues.
Teleflex MedicalJan 14, 2019 - Lower riskMedical device
Becton Dickinson & Co. recalls BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX
Becton Dickinson recalls BD MAX Enteric Bacterial Panel (Catalog 442963) due to false negative results when testing for ETEC and Plesiomonas shigelloides. Affected units may not detect infections accurately.
Becton DickinsonJan 14, 2019 - Use cautionMedical device
Shimadzu Medical Systems Usa Com recalls TRINIAS for diagnostic imaging and interventional procedures in cardiac angiography, neurovascular angiography,
Shimadzu recalls TRINIAS medical imaging devices for potential fluoroscopy errors and image corruption during cardiac/neurovascular procedures. Affected units have specific serial numbers.
Shimadzu Medical SystemsJan 14, 2019 - Use cautionMedical device
Arthrex, Inc. recalls Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous
Arthrex recalls oval surgical burrs (AR-8550OBT) that may overheat during arthroscopic procedures. Affected units have specific lot numbers and expiration dates.
ArthrexJan 14, 2019 - Use cautionMedical device
Shimadzu Medical Systems Usa Com recalls BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic
Shimadzu recalls specific digital angiography systems that may abnormally terminate after a fluoroscopy error during patient registration. Affected units require service intervention to prevent disruption of medical procedures.
Shimadzu Medical SystemsJan 14, 2019 - Lower riskFood
Century Snacks LLC recalls Snak Club Praline Pecans Made With Cane Sugar NET Wt. 2.25 oz (64 g) Produced By: Century Snack Commerce, CA 90040
Century Snacks recalls praline pecans labeled as pecans but actually contain almonds. This mislabeling could cause confusion for consumers expecting pecans.
Century SnacksJan 14, 2019 - Use cautionVehicle
MERCEDES-BENZ AMG GT (2017) recall — Communication
Mercedes-Benz recalls 2017 AMG GTs with software fault that may delay emergency responders by giving wrong vehicle location. Owners can get free software update via over-the-air remote update.
Mercedes-BenzJan 11, 2019 - Use cautionVehicle
MERCEDES-BENZ GLC350E (2019) recall — Seat Belts
Mercedes-Benz recalls 2019 GLC350e vehicles with faulty seat belts that may not deploy during crashes, increasing injury risk. Owners should contact MBUSA for free front seat belt buckle repairs.
Mercedes-BenzJan 11, 2019 - Use cautionVehicle
THOR MOTOR COACH OMNI (2020) recall — Seats
Thor Motor Coach is recalling 2019-2020 Omni motorhomes with potentially weak seat recliner mechanisms that could not properly restrain occupants during crashes, increasing injury risk. Affected owners should contact Ford or TMC for free seat replacements.
Thor Motor CoachJan 11, 2019
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