Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,099 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,099 in last 12 months

Showing 8601–8620 of 51,386 recalls

Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Draeger Medical, Inc.

Recalled Item: Carina Sub-Acute Care Ventilator Recalled by Draeger Medical, Inc. Due to...

The Issue: Presence of polyether polyurethane (PE-PUR) and emission of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX S Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX C+ Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Olympus Corporation of the Americas

Recalled Item: The Air/Water Valve is provided/used with the following Endoscopes:...

The Issue: The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...

The Issue: There is a potential for a product packaging non-conformity issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 11, 2023· Ascend Laboratories, LLC

Recalled Item: Fingolimod Capsules Recalled by Ascend Laboratories, LLC Due to Failed...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2023· Sagent Pharmaceuticals

Recalled Item: Oxacillin for Injection Recalled by Sagent Pharmaceuticals Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2023· Sagent Pharmaceuticals

Recalled Item: Oxacillin for Injection Recalled by Sagent Pharmaceuticals Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2023· Sagent Pharmaceuticals

Recalled Item: Oxacillin for Injection Recalled by Sagent Pharmaceuticals Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Tiagabine Hydrochloride Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: Failed Impurities: Out of Specification (OOS) result observed during Related...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2023· New England Life Care, Inc. dba Advanced Compounding Solutions

Recalled Item: PHENYLephrine HCl 10mg added to 0.9% Sodium Chloride 250mL Recalled by New...

The Issue: CGMP Violations- that spaces adjacent to the production area may have been...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2023· New England Life Care, Inc. dba Advanced Compounding Solutions

Recalled Item: SUCCINYLcholine Chloride 200 mg/10mL (20 mg/mL) Recalled by New England Life...

The Issue: CGMP Violations- that spaces adjacent to the production area may have been...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2023· New England Life Care, Inc. dba Advanced Compounding Solutions

Recalled Item: ROcuronium Bromide 50 mg/5 mL ( 10 mg/mL) Recalled by New England Life Care,...

The Issue: CGMP Violations- that spaces adjacent to the production area may have been...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund