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All Recalls

Every Other Recall

Sorted by most recent. Click any recall for full details and safety information.

21,986 recalls
High RiskFDA
Acclarent, Inc.
TruDi NAV Suction, TDNS070Z, 70 Degree Tip Angle (01) 10705031245884
Medical Devices·0 affected·Mar 6, 2019
High RiskFDA
Acclarent, Inc.
TruDi NAV Suction, TDNS090Z, 90 Degree Tip Angle, (01) 10705031245891
Medical Devices·0 affected·Mar 6, 2019
High RiskFDA
Becton Dickinson & Company
Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07
Medical Devices·21,220 affected·Mar 5, 2019
RecallFDA
Avkare Inc.
Oxybutynin Chloride Extended-Release Tablets USP 10 mg, a) 100 tablets (NDC 42291-634-01) and b) 500 tablets (NDC 42291-634-50) bottles, ...
Oral Drugs·2,947 affected·Mar 1, 2019
High RiskFDA
Apotex Inc.
Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged as 84 Tablets Blist...
Oral Drugs·82,705 affected·Mar 1, 2019
High RiskFDA
Zimmer Biomet, Inc.
Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile Titanium. Accessory to total hip implant Item Number: 103531 ...
Medical Implants·809 affected·Mar 1, 2019
High RiskFDA
Integra Limited
Integra bioBLOCK Resorbable subtaler Implant, 10mm Catalog Number: 40010 - Product Usage: The bioBLOCK Implant is indicated for intern...
Medical Implants·232 affected·Mar 1, 2019
High RiskFDA
Zimmer Biomet, Inc.
Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile Titanium, Accessory to total hip implant Item Number: 103533 ...
Medical Implants·809 affected·Mar 1, 2019
High RiskFDA
Integra Limited
Integra bioBLOCK Resorbable subtaler Implant, 12mm Catalog Number: 040012 - Product Usage: The bioBLOCK Implant is indicated for inter...
Medical Implants·232 affected·Mar 1, 2019
High RiskFDA
Integra Limited
Integra bioBLOCK Resorbable subtaler Implant, 11mm Catalog Number: 040011 - Product Usage: The bioBLOCK Implant is indicated for inter...
Medical Implants·232 affected·Mar 1, 2019
High RiskFDA
Camber Pharmaceuticals Inc
Losartan Potassium Tablets USP, 50 mg, Rx only, a) 30 count (NDC 31722-701-30), b) 90 count (NDC 31722-701-90), c) 1000 count (NDC 31722-...
Oral Drugs·69,712 affected·Feb 28, 2019
High RiskFDA
Camber Pharmaceuticals Inc
Losartan Potassium Tablets USP, 100 mg, Rx only, a) 30 count (NDC 31722-702-30), b) 90 count (NDC 31722-702-30), c) 1000 count (NDC 31722...
Oral Drugs·683,641 affected·Feb 28, 2019
High RiskFDA
Camber Pharmaceuticals Inc
Losartan Potassium Tablets USP, 25 mg, Rx only, a) 90 count (NDC 31722-700-90), b) 500 count (NDC 31722-700-05) and c) 1000 count (NDC 31...
Oral Drugs·351,732 affected·Feb 28, 2019
RecallFDA
Jubilant Cadista Pharmaceuticals, Inc.
BuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg, a) 30 count (NDC 59746- 758-30) & b) 90 count (NDC 59746-758-90) bottl...
Oral Drugs·3,072 affected·Feb 28, 2019
High RiskFDA
Philips North America, Llc
Omnidiagnost Classic, Product Codes 70859, 708023, 708024, 708025 Product Usage: The Philips OmniDiagnost is a multi-functional, univ...
Diagnostic Devices·1,696 affected·Feb 28, 2019
High RiskFDA
Philips North America, Llc
URODiagnost Eleva, Product codes 708026, 708027, 708028 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ra...
Diagnostic Devices·1,969 affected·Feb 28, 2019
High RiskFDA
Biomet 3i, Llc
CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM, Item Number ILDAN3 - Product Usage: BIOMET3i Restorative products are intended for use as an a...
Medical Implants·2 affected·Feb 26, 2019
High RiskFDA
Biomet 3i, Llc
CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM, Item Number IIAT3 - Product Usage: BIOMET3i Restorative products are intended for use as...
Medical Implants·6 affected·Feb 26, 2019
High RiskFDA
Biomet 3i, Llc
CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM, Item Number IEDAT3 - Product Usage: BIOMET3i Restorative products are intended for use as...
Medical Implants·17 affected·Feb 26, 2019
High RiskFDA
Biomet 3i, Llc
CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM, Item Number IEDAN3 - Product Usage: BIOMET3i Restorative products are intended for use as an a...
Medical Implants·3 affected·Feb 26, 2019
RecallUSDA
Mcallen Cold Storage, Ltd.
McAllen Cold Storage, Ltd. Recalls Siluriformes Fish Products Produced Without Benefit Of Inspection
Poultry·0 affected·Feb 26, 2019
RecallUSDA
Mcallen Cold Storage, Ltd.
Mcallen Cold Storage, Ltd. retira productos de pescado siluriformes producidos sin el beneficio de la inspección
Meat & Poultry·0 affected·Feb 26, 2019
High RiskFDA
Albertsons Companies Llc
Signature Caf¿ Tomato Basil Bisque Soup: polypropylene cups with linear low density polyethylene caps, and with plastic film seal. NET ...
Produce·500 affected·Feb 25, 2019
RecallFDA
Cook Medical Incorporated
Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-C ELECT-PT Product Us...
Medical Implants·91,731 affected·Feb 25, 2019
RecallFDA
Cook Medical Incorporated
Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach, Catalog Number GTCFS-65-1-JUG-CELECT-PT Product Usage: The Cook...
Medical Implants·91,731 affected·Feb 25, 2019
RecallFDA
Cook Medical Incorporated
Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-TULIP Product Usage: The Gu...
Medical Implants·91,731 affected·Feb 25, 2019
RecallFDA
Nidek, Inc.
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image capture of endothelium...
Medical Devices·13 affected·Feb 25, 2019
RecallFDA
Cook Medical Incorporated
Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach, Catalog Number IGTCFS-65-1-FEM-TU LIP Product Usage: The Gunther Tulip...
Medical Implants·91,731 affected·Feb 25, 2019
High RiskFDA
Ascend Laboratories Llc
Tamsulosin Hydrochloride Capsules, USP, 0.4 mg, 500-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, I...
Oral Drugs·3,072 affected·Feb 22, 2019
High RiskFDA
Keystone Dental Inc
Paltop Premium Surgical Kit-containing the 1.25mm Hex Driver For surgical and restorative applications prosthetic devices, such as artif...
Medical Implants·13 affected·Feb 22, 2019
High RiskFDA
Keystone Dental Inc
Paltop Fully Guided Surgical Kit- containing the 1.25mm Hex Driver For surgical and restorative applications prosthetic devices, such as...
Medical Implants·1 affected·Feb 22, 2019
RecallUSDA
Unknown
Fulton Seafood Inc. Recalls Siluriformes Products Produced Without Benefit of Inspection
Poultry·0 affected·Feb 22, 2019
RecallUSDA
Unknown
Fulton Seafood Inc. retira productos siluriformes producidos sin el beneficio de la inspección
Seafood·0 affected·Feb 22, 2019
RecallUSDA
Unknown
TV Food LLC. Recalls Siluriformes Products Produced Without Benefit of Inspection
Poultry·0 affected·Feb 22, 2019
RecallUSDA
Unknown
TV Food LLC. retira productos siluriformes producidos sin el beneficio de la inspección
Seafood·0 affected·Feb 22, 2019
RecallCPSC
Dive Right In Scuba And Online Scuba Stores Nationwide And Online At Www.divegearexpress.com And Www.shearwater.com From June 2017 Through November 2018 For About $350.
Shearwater Recalls Diving Transmitters Due to Drowning Hazard
Consumer Products·900 affected·Feb 21, 2019
RecallFDA
Lannett Company Inc.
Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 191...
Oral Drugs·14,448 affected·Feb 21, 2019
High RiskFDA
Arthrocare Corporation
Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971
Medical Devices·15,559 affected·Feb 21, 2019
High RiskFDA
Abbott Laboratories
CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automated hematology analyzer intended for in-vitro diagnostic us...
Diagnostic Devices·6,353 affected·Feb 20, 2019
High RiskFDA
Ortho-clinical Diagnostics
VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in the in vitro quantitative, semi-quantitative, and qualita...
Diagnostic Devices·45 affected·Feb 20, 2019
High RiskFDA
Ortho-clinical Diagnostics
VITROS ECi Immunodiagnostic System Refurbished Product Code: 6801059 For use in the in vitro quantitative, semi-quantitative, and qu...
Diagnostic Devices·25 affected·Feb 20, 2019
RecallFDA
Amerigen Pharmaceuticals Inc.
Temozolomide Capsules, 5 mg, packaged in a) 5-count bottle (NDC 43975-252-05) b) 14-count bottle (NDC 43975-252-14), Rx only, Mfd. by: St...
Oral Drugs·2,413 affected·Feb 19, 2019
High RiskFDA
Smith & Nephew, Inc.
smith&nephew SMF(TM) HIGH OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1H SIZE, STEM, REF 713552511
Medical Devices·9 affected·Feb 19, 2019
High RiskFDA
Philips Medical Systems Nederlands
Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The Allura Xper FD Serie...
Diagnostic Devices·7,209 affected·Feb 19, 2019
High RiskFDA
Smith & Nephew, Inc.
smith&nephew SMF(TM) STANDARD OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1 SIZE, STEM, REF 713552510
Medical Devices·58 affected·Feb 19, 2019
High RiskFDA
Philips Medical Systems Nederlands
Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 722002 Allura Xper FD10 F 722003 Allura Xper FD10 722005...
Diagnostic Devices·7,209 affected·Feb 19, 2019
High RiskFDA
Gasco Industrial, Corp.
Gasc¿ Tomato Red Food Color, Net Contents: 5 gal (640 fl. oz)
Produce·35 affected·Feb 15, 2019
High RiskFDA
Alere San Diego, Inc.
Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d - Product Usage: Th...
Diabetes Devices·186 affected·Feb 15, 2019