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. 2,401 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,401 in last 12 months

Showing 4450144520 of 52,000 recalls

Medical DeviceMarch 19, 2014· Zimmer, Inc.

Recalled Item: DROP LOK" Knee Brace***LATEX FREE" Product Usage: Used in the treatment...

The Issue: During a transfer of products from a recently shutdown facility, the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2014· CareFusion 303, Inc.

Recalled Item: SmartSite Extension Set Recalled by CareFusion 303, Inc. Due to...

The Issue: Disconnections and leakages at the connection of the smallbore tubing and...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2014· Glenmark Generics Inc., USA

Recalled Item: Ranitidine Tablets USP Recalled by Glenmark Generics Inc., USA Due to...

The Issue: Presence of Foreign Tablets/Capsules: Recall is due to a pharmacist...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: JK Bariatric Beds Recalled by SCM True Air Technologies LLC Due to The firm...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: MaXair True Low Air Loss Mattress Replacement System Recalled by SCM True...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: ECATS E 850 Bariatric Bed Recalled by SCM True Air Technologies LLC Due to...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· Energizer Personal Care

Recalled Item: Playtex Nurser Deluxe Double Electric Breast Pump Recalled by Energizer...

The Issue: Some of the power adapters outer casings may become loose and separate,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 2.5MM Aggressive Blade Known as a Sinuscopic Shaver Blade Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the single use 2.5MM Aggressive...

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

Class II — Potential Health HazardOngoing
DrugMarch 17, 2014· John W Hollis Inc

Recalled Item: Papaverine 60 mg Recalled by John W Hollis Inc Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Expiration Date; Expiration date is earlier than listed...

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2014· John W Hollis Inc

Recalled Item: Polidocanol 3% Solution Recalled by John W Hollis Inc Due to Presence of...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2014· John W Hollis Inc

Recalled Item: Phosphatidylcholine Solution for Injection Recalled by John W Hollis Inc Due...

The Issue: Labeling: Incorrect Expiration Date; Expiration date is earlier than listed...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2014· John W Hollis Inc

Recalled Item: Polidocanol 1% Solution Recalled by John W Hollis Inc Due to Labeling:...

The Issue: Labeling: Incorrect Expiration Date; Expiration date is earlier than listed...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 17, 2014· Arjo Hospital Equipment AB

Recalled Item: ArjoHuntleigh Contoura C1000 series beds are designed to accommodate...

The Issue: There is a low but existing entrapment risk for a patient being treated on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Remel Inc

Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent contained...

The Issue: A reagent contained within the product may return false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Philips Medical Systems, Inc.

Recalled Item: Digital Diagnost Recalled by Philips Medical Systems, Inc. Due to The...

The Issue: The footboard of Patient support for stitching can be fixed in upper...

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

Class II — Potential Health HazardOngoing