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. 2,509 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,509 in last 12 months

Showing 2272122740 of 52,000 recalls

Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 2 pc Full Wrap Vest & Kilt Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Front/Back Apron with Stretch Velcro Closure Recalled by Burlington Medical,...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 2 pc Full Overlap Vest & Kilt Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Support Belt Apron Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Apron Velcro Closure Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Hood Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Apron with Quick Drop Velcro Closure (no elastic) Recalled by...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Vest Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Overlap Vest Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Panels Lipid Panel test strip: IVD Lipid Panel Test Recalled by Polymer...

The Issue: The MEMo chips provided with lot P901 may be mislabeled, the MEMo Chip may...

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

Class III — Low RiskOngoing
DrugJune 7, 2019· PharMEDium Services, LLC

Recalled Item: Hydromorphone HCl in 0.9% sodium chloride Recalled by PharMEDium Services,...

The Issue: Incorrect Product Formulation; Firm's customer resource center (CRC)...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 7, 2019· Akorn Inc

Recalled Item: Myorisan (isotretinoin capsules Recalled by Akorn Inc Due to Labeling: Label...

The Issue: Labeling: Label mix-up: Product secondary carton erroneously states 40mg...

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

Class III — Low RiskOngoing
Refund
DrugJune 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 100 mg TABLET BULK 90 count bottles Recalled by Teva...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2019· Skeletal Kinetics, Llc

Recalled Item: OsteoVation Recalled by Skeletal Kinetics, Llc Due to A discrepancy was...

The Issue: A discrepancy was found between the Mixing Instruction Card and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q.zen ceiling-Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee floor -Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q zeego ---Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing