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 27021–27040 of 29,188 recalls
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rostorelle L Recalled by Coloplast Manufacturing US, LLC Due to Mislabeling
The Issue: Coloplast is recalling one lot of Restorelle L prosthesis because it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Staple Remover Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmented Cylinder Applicator Set Recalled by Varian Medical Systems, Inc....
The Issue: Segmented cylinder applicator set may slip during treatment, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KayserBetten model IDA beds Product Usage: BED Recalled by mobility...
The Issue: Some joints on the doors of a limited number of IDA beds may loosen or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3536A Recalled by...
The Issue: Device Operating on Battery Power May Shutdown without Warning if exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman(R) Collins Radioparent Sternal Blade Nylon Recalled by Symmetry...
The Issue: There is a possibility that the Collins Radioparent Sternal Blades Nylon may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.