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.
Showing 25061–25080 of 29,188 recalls
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroglobulin (1D4) is a mouse anti-human monoclonal antibody produced as...
The Issue: Bond Ready to Use Primary Antibody Thyroglobulin does not function as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...
The Issue: High priority alert icon was not displayed in the Study List when there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...
The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Adult Universal Ventilator Circuit Recalled by Teleflex Medical...
The Issue: Product is being recalled due to complaints that the inspiratory and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) -...
The Issue: Patients and caregivers are instructed that if a battery does not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...
The Issue: DePuy Synthes is initiating a recall of certain lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...
The Issue: Test Strips may report an inaccurately low INR result. Several patients had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDFILL Syringe Strip Recalled by Baxter Corporation Englewood Due to...
The Issue: Possible breach in sterile barrier for inner and outer bags of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...
The Issue: This Lot has variations in melting temperature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...
The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...
The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...
The Issue: When using a specific plan update workflow in combination with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...
The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...
The Issue: A stock check revealed broken glass fibers between the connector and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.