Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,963 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,963 in last 12 months

Showing 1550115520 of 52,000 recalls

DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Octreotide Acetate Injection 50 mcg/mL Recalled by Teva Pharmaceuticals USA...

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 29, 2021· Novel Laboratories, Inc. d.b.a LUPIN

Recalled Item: GaviLyteTM - C PEG-3350 (240g) and Electrolytes for Oral Solution Recalled...

The Issue: Failed Stability Specification; Out of specification for Osmolarity

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Haloperidol Decanoate Injection 100 mg/mL Recalled by Teva Pharmaceuticals...

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 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

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 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA 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 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Amikacin Sulfate Injection USP 1 gram/4mL (250mg/ML) Recalled by Teva...

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 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Alprostadil Injection USP Recalled by Teva Pharmaceuticals USA Due to Lack...

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 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...

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 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Vecuronium Bromide for Injection 10 mg Recalled by Teva Pharmaceuticals USA...

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 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA 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 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Ethosuximide Oral Solution USP 250 mg/5 mL Recalled by PAI Holdings, LLC....

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Venlafaxine Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Cimetidine Hydrochloride Oral Solution 300 mg/5 mL Recalled by PAI Holdings,...

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 29, 2021· Mizuho OSI

Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...

The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Sentinel CH SpA

Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...

The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...

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

Class III — Low RiskOngoing
Medical DeviceJuly 29, 2021· Lymol Medical Corporation

Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...

The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: OASIS MRI System Recalled by Hitachi Healthcare Americas Corporation Due to...

The Issue: There was no label on the pad packaging or notification in the user manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: ECHELON MRI System Recalled by Hitachi Healthcare Americas Corporation Due...

The Issue: There was no label on the pad packaging or notification in the user manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...

The Issue: There was no label on the pad packaging or notification in the user manual...

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

Class II — Potential Health HazardOngoing