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.
Showing 27861–27880 of 29,188 recalls
Recalled Item: Posey Biothane Restraint Cuffs Recalled by J T Posey Company Due to The firm...
The Issue: The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Overhead Rail System Recalled by Hill-Rom, Inc. Due to Liko/Hill-Rom to...
The Issue: Liko/Hill-Rom to date has received two reports from facilities alleging that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical RUMI Arch Recalled by Cooper Surgical, Inc. Due to Excessive...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...
The Issue: This notice is being provided in follow up to the field correction initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Software Version R2.0.2 Product Usage: This system...
The Issue: With Digital Diagnost R2.0.2 a mirrored "R in a circle" is burnt into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous Fixation System (IFS) 1.7 mm Recalled by Orthohelix Surgical...
The Issue: The firm was notified by a customer that there was a burr on the inside end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Stationary radiographic system Recalled by Philips...
The Issue: When the operator for a wall stand view selects an "image rotation"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Recalled by Cordis Corporation Due to Affected lots of Cordis ExoSeal...
The Issue: Affected lots of Cordis ExoSeal (TM) VCD have been sterilized using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Single Channel Infusion Pumps with Hospira MedNet...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Single Channel Infusion Pumps with Plug-and-Play Modules that...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Single Channel Infusion Pumps with Hospira Mednet Software Recalled...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiOM Rechargeable Li Ion 22.2 V Battery and BiOM Lithium Recalled by iwalk...
The Issue: Battery may over-heat during charging and smoke
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the AU8500 Clinical Chemistry Analyzer because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiples Anspach Micro Curved Attachments (MCA) and Curved Burr Support...
The Issue: During a recent review of documentation Anspach determined that the current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...
The Issue: A manufacturing defect has been identified which could results in the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that...
The Issue: Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlant Recalled by Kerr Corporation Due to The firm initiated the recall...
The Issue: The firm initiated the recall becaue disturbing the BioPlant product soon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...
The Issue: A manufacturing defect has been identified which could results in the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quasar MD is an infrared LED lamp that is labeled Recalled by Quasar...
The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.