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
35,025 found- Stop using nowDrug
Je Dois Lavoir LLC recalls 365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL
FDA recalls Je Dois Lavoir's 365 SKINNY High Intensity Capsules due to undeclared sibutramine, a withdrawn drug with safety concerns. Consumers should stop using affected lots.
Je Dois LavoirAug 2, 2021 - Lower riskFood
Golden Natural Products recalls Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and Golden Natural
Golden Natural Products recalls dried apricots containing undeclared sulfites. Consumers should check product labels for lot number GC005 and contact the company for details.
Golden Natural ProductsAug 2, 2021 - Use cautionVehicle
WABASH NATIONAL VAN (2019) recall — Fuel System, Gasoline
Wabash recalls 2018-2022 Van Trailers with potential fuel tank detachment causing crash risk. Owners must contact for free bracket repair.
WabashJul 30, 2021 - Use cautionVehicle
FORD TRANSIT CONNECT (2021) recall — Seat Belts
Ford is recalling 2021 Transit Connect vehicles with front passenger seat belt automatic locking retractors that may deactivate early, risking child restraint system failure during crashes. Owners must have seat belts inspected and replaced free by dealers.
FordJul 30, 2021 - Use cautionVehicle
ENTEGRA ANTHEM (2020) recall — Fuel System, Diesel
Entegra is recalling 2018-2022 Anthem, Aspire, Insignia, and Reatta XL Class A vehicles due to potential fuel leaks that could cause fire if near ignition sources.
EntegraJul 30, 2021 - Use cautionMedical device
Getinge Dominican Republic SA recalls Arjo Disposable Repositioning Sling, Model AHD001
Getinge recalls Arjo Disposable Repositioning Sling Model AHD001 due to trip hazard from sling loop straps. Affected units include specific lots listed in the recall notice.
GetingeJul 30, 2021 - Lower riskMedical device
Paragon 28, Inc. recalls Phantom Nail System, Drill, 4.6 x 300mm, Cannulated, 3/16" Sq. Connection p28 P99-110-4630
Paragon 28 recalls Phantom Nail System Drills with thin wall condition that may fracture, risking injury. Affected models include P99-110-4630.
Paragon 28Jul 30, 2021 - Use cautionMedical device
Philips North America Llc recalls Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system
Philips recalls Ingenia Elition X-MRI systems with faulty pressure relief valve that may release helium gas, causing injury. Affected units have specific model and serial numbers. Consumers should contact Philips for details.
PhilipsJul 30, 2021 - Lower riskMedical device
Leica Microsystems, Inc. recalls BOND Ready-To-Use Primary Antibody CDX2 (EP25), REF PA0375
Leica Microsystems recalls BOND Ready-To-Use Primary Antibody CDX2 (EP25) REF PA0375 due to potential performance issues. Affected units may not function correctly as per instructions.
LeicaJul 30, 2021 - Lower riskDrug
Noven Pharmaceuticals Inc recalls Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg per day, 50/140 Twice Weekly, Rx Only a) 2
Noven Pharmaceuticals recalls specific Combipatch hormone patches due to stability issues. These patches may not function correctly over time, potentially affecting hormone levels. Stop using and contact for details.
NovenJul 30, 2021 - Stop using nowDrug
Custopharm, Inc. recalls FLUDARABINE PHOSPHATE FOR INJECTION, USP, 50 mg per vial, Single dose vial, Rx Only, Mfd for: Leucadia Pharmaceuticals
Custopharm recalls 50mg FLUDARABINE PHOS: manufacturing had microbial issues. Stop using if you have this injection. Details: NDC 24201-237-01, Lot 31327913C, Exp 10/2022.
CustopharmJul 30, 2021 - Lower riskDrug
BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy recalls Succinylcholine Chloride 100 mg/5 mL (20 mg/mL), 5 mL Syringes, Rx only, For IV Use only, BayCare Central Pharmacy,
BayCare Central Pharmacy recalls 100 mg/5 mL succinylcholine chloride syringes due to lack of sterility assurance. This could lead to infections if used improperly. Affected lots: SUCC10020210624 (expiring 09/22/2021).
BayCare Central PharmacyJul 30, 2021 - Lower riskMeat & poultry
Greater Omaha Packing Recalls Raw Beef Products Due to Possible E. Coli O157:H7 Contamination
USDA recalls 295,236 pounds of raw beef products from Greater Omaha Packing due to possible E. coli O157:H7 contamination. Products may cause severe illness, especially in children under 5 and older adults.
Greater Omaha PackingJul 29, 2021 - Use cautionVehicle
BMW X5 (2018) recall — Fuel System, Diesel
BMW recalls certain 2014-2018 diesel vehicles due to potential fuel pump failure causing engine stalls and crash risks. Owners must have the high-pressure fuel pump replaced at no cost by dealers.
BMWJul 29, 2021 - Use cautionVehicle
CHEVROLET TAHOE (2021) recall — Service Brakes, Hydraulic
General Motors recalls 2021 Chevrolet Tahoe vehicles with potentially compromised braking performance due to incorrect brake system calibration. Owners should contact dealers for free recalibration.
ChevroletJul 29, 2021 - Use cautionVehicle
SUBARU LEGACY (2020) recall — Fuel System, Gasoline
Subaru is recalling 2020 Legacy vehicles with potential fuel pump failure causing engine stalls and crash risk. Owners must have fuel pump replaced free by dealers.
SubaruJul 29, 2021 - Use cautionVehicle
SPARTAN K2 (2020) recall — Electrical System
Shyft Group recalls 2020 Spartan K2 RVs with potential instrument cluster blanking, risking speed and warning light loss during driving. Owners must update software and secure duct work for free.
Shyft GroupJul 29, 2021 - Lower riskVehicle
LAND ROVER DEFENDER (2020) recall — Equipment
Land Rover is recalling 2020-2021 Defender vehicles with incorrect child seat restraint info in owner's manual. This may cause improper child seat installation and injury risk in crashes. Owners receive updated manual instructions via mail.
Land RoverJul 29, 2021 - Use cautionVehicle
CHEVROLET SILVERADO 2500 (2020) recall — Tires
Chevrolet is recalling 2020-2021 Silverado 2500 models with specific spare tires that may cause ABS system failure, increasing crash risk. Owners must contact GM for free repairs.
ChevroletJul 29, 2021 - Lower riskMedical device
Mizuho OSI recalls HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
Mizuho OSI recalls HANA/PROFx Classic Femoral Hook Right Ref 6850-144 due to incorrect model numbering. Affected units have a specific batch code and require verification.
Mizuho OSIJul 29, 2021 - Lower riskMedical device
Lymol Medical Corporation recalls LYMOL Medical Elite X Class Rigid Bronchoscope System, Part No. BD2410, BB2701, BB2702, BB2401, BB2402, BA2700, BT2000,
Lymol Medical recalls Elite X Class Rigid Bronchoscope Systems due to outdated reprocessing instructions not being sent to all users. Affected models include BD2410, BB2701, and others. No immediate action needed but ensure updated instructions are followed.
Lymol MedicalJul 29, 2021 - Lower riskMedical device
Hitachi Healthcare Americas Corporation recalls OASIS MRI System
Hitachi Healthcare recalls OAS: MRI systems M001-M329 and M951 due to missing label indicating dry natural rubber pads, which may not meet federal safety standards.
Hitachi HealthcareJul 29, 2021 - Lower riskMedical device
Sentinel CH SpA recalls Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of
Sentinel CH recalls Alinity c CRP Vario Calibrator Kit (ref 07P5605) due to incorrect vial labeling, which may prevent successful calibration of cardiac tests on Alinity c analyzers.
Sentinel CHJul 29, 2021 - Lower riskDrug
Teligent Pharma, Inc. recalls Erythromycin Topical Solution USP, 2%, 60mL bottle, Rx only, Teligent Pharma, Inc. Buena, NJ 08310, NDC 52565-027-59
Teligent Pharma recalls 2% Erythromycin Topical Solution 60mL bottles (Rx only) due to possible container seal failure. Affected lots: 14892 (expiring 1/2022).
Teligent PharmaJul 29, 2021 - Use cautionDrug
Novel Laboratories, Inc. d.b.a LUPIN recalls GaviLyteTM - C PEG-3350 (240g) and Electrolytes for Oral Solution, USP with Flavor Pack Manufactured by Novel
Lupin recalls GaviLyte-C PEG-3350 oral solution due to failed stability specifications and out-of-specification osmolarity. Check your lot number.
LupinJul 29, 2021 - Lower riskDrug
The Harvard Drug Group recalls Entacapone Tablets, USP, 200 mg, Rx only, 30 Tablets per unit dose cartons, Distributed by: Major Pharmaceuticals,
Harvard Drug Group recalls 200mg Entacapone Tablets due to failed dissolution specifications. Affected units have specific NDC and lot numbers. Consumers should contact the manufacturer for details.
The Harvard Drug GroupJul 29, 2021 - Lower riskDrug
Teligent Pharma, Inc. recalls Lidocaine Ointment USP, 5% Rx Only, Net Wt 35.44 g(1 1/4 oz)packaged in a laminat tube, Teligent Pharma, Inc. Buena,
Teligent Pharma recalls 5% Lidocaine Ointment USP (1 1/4 oz) due to failed viscosity specifications. This may affect product consistency and safety. Check NDC 52565-008-14 and lot numbers for affected items.
Teligent PharmaJul 29, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by:
Sun Pharmaceutical recalls Venlafaxine 50mg tablets due to foreign tablets found in some bottles. Consumers should check product labels and contact Sun Pharmaceutical for details.
Sun Pharmaceutical Industries IncJul 29, 2021 - UnratedDrug
Teva Pharmaceuticals USA recalls Cyclobenzaprine Hydrochloride Tablets, 7.5mg, 100 count tablets per bottle, Rx Only, Manufactured by: Actavis
Teva Pharmaceuticals USA recalls 7.5mg cyclobenzaprine tablets due to potential microbial contamination in an excipient batch. Affected products have NDC 70199-014-01 or 1408822A, expiring 08/2023. No specific remedy is stated in the recall notice.
Teva Pharmaceuticals USAJul 29, 2021 - Lower riskDrug
PAI Holdings, LLC. dba Pharmaceutical Associates Inc recalls Ethosuximide Oral Solution USP 250 mg/5 mL, 16 fl oz (473 mL), Rx ONLY, Pharmaceutical Associates, Inc. Greenville, SC
Pharmaceutical Associates recalls Ethosuximide Oral Solution (250 mg/5 mL) due to potential carryover of Senna Syrup. This prescription medication may cause unintended effects if used without proper cleaning.
Pharmaceutical AssociatesJul 29, 2021
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