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. 1,034 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,034 in last 12 months

Showing 23161–23180 of 52,000 recalls

Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PICC Line Accessory Kit CVI4285 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: IV START KIT IV8440 Recalled by Centurion Medical Products Corporation Due...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: VANTEX 7FR Recalled by Centurion Medical Products Corporation Due to Firm...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: OR VANTEX 7FR 3L 16CM CVC ECVC6665 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450A Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PORT AND IO ACCESS DRESSING KIT DT15780A Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· Legacy Pharmaceutical Packaging LLC

Recalled Item: Losartan Potassium Tablets Recalled by Legacy Pharmaceutical Packaging LLC...

The Issue: CGMP Deviations: Detection of trace amounts of N-Methylnitrosobutyric acid...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· MAJOR PHARMACEUTICALS

Recalled Item: DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS Recalled by MAJOR PHARMACEUTICALS...

The Issue: cGMP deviations: Product was exposed above 50% relative humidity levels...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Mullein leaf c/s Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Goldenseal herb c/s Recalled by AmeriHerb International Inc Due to Potential...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Lemon balm leaf c/s Recalled by AmeriHerb International Inc Due to Potential...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Parsley flakes Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Dill weed c/s Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Blessed thistle herb c/s Recalled by AmeriHerb International Inc Due to...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 23, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Precision Integrated System 120V Recalled by CooperSurgical, Inc. Due...

The Issue: 2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC Kit Product Code: ASK 45541 RWJ4 Recalled by Arrow International...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC Kit Product Code: ASK 45552 RWJ4 Recalled by Arrow International...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing