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. 1,110 recalls have been distributed to Tennessee in the last 12 months.
Showing 7161–7180 of 29,188 recalls
Recalled Item: Veritas Advanced Infusion Packs Recalled by Johnson & Johnson Surgical...
The Issue: Weld protrusion/physical gap between the housing and phaco pack cover, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Use Packs Recalled by Johnson & Johnson Surgical Vision, Inc. Due to...
The Issue: Weld protrusion/physical gap between the housing and phaco pack cover, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobiCT-32 AIRO Mobile CT Scanner Recalled by Mobius Imaging, LLC Due to...
The Issue: Stryker received one report of an injury to an untrained user that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 4 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 6 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 8 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 7 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 5 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 3 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invisalign Express 10 Invisalign System Comprehensive Recalled by Align...
The Issue: 3D orthodontic planning software has a defect that leads to an issue where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra Brachy radiation therapy planning system software. Recalled by...
The Issue: A reconstruction error may occur when using the Catheter Bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIP KIT Recalled by Cardiac Assist, Inc Due to A software update (v1.1.5)...
The Issue: A software update (v1.1.5) has been developed to address the issue of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denticator PICK-A-DENT Recalled by Young Dental Manufacturing I, LLC Due to...
The Issue: mislabeled product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalon Monofilament Nylon Suture: (1) 88861741-11 DERMALON* 6-0 BLU 45CM...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ti-Cron Coated Braided Polyester Suture Product Description 88862775-31...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Surgical Patties Recalled by Integra LifeSciences Corp. Due to...
The Issue: Integra LifeSciences identified that one lot was released with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.