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. 2,492 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,492 in last 12 months

Showing 2694126960 of 52,000 recalls

Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2018· Medline Industries Inc (Northpoint Services)

Recalled Item: READYFLUSH PROTECT with Dimethicone (3.2%) Recalled by Medline Industries...

The Issue: Microbial Contamination of a Non-Sterile Product.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2018· Lake Michigan Distilling Co LLC

Recalled Item: Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol Recalled by Lake...

The Issue: Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...

The Issue: The block used to connect the patient pallet to the couch may be assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: REPLANT 5.0mmD ABUTMENT Recalled by Implant Direct Sybron Manufacturing, LLC...

The Issue: Due to out of specification, the clinician would not be able to fit and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...

The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Qiagen Sciences, Inc.

Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...

The Issue: Potential for control line not appearing on the test strip

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 18, 2018· OMNIlife science Inc.

Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...

The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.

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

Class II — Potential Health HazardOngoing
FoodMay 18, 2018· Pious Lion

Recalled Item: Pious Lion Pure Premium Potent White Maeng DA Recalled by Pious Lion Due to...

The Issue: The firm was notified by the North Carolina Dept. of Agriculture that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 18, 2018· Pious Lion

Recalled Item: Pious Lion Pure Premium Potent Limited Release Pink Bali Recalled by Pious...

The Issue: The firm was notified by the North Carolina Dept. of Agriculture that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 17, 2018· Ziyad Brothers Importing, Inc.

Recalled Item: Ziyad Brand Tahini Recalled by Ziyad Brothers Importing, Inc. Due to...

The Issue: Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
DrugMay 17, 2018· Shoreside Enterprises Inc.

Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...

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

Class I — Serious Health HazardOngoing
Refund