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. 2,645 recalls have been distributed to Tennessee in the last 12 months.
Showing 12861–12880 of 29,188 recalls
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear Capillary Dialyzer 300 Recalled by Baxter Healthcare Corporation...
The Issue: There is the potential presence of particular matter in the header caps of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PneumoDart Recalled by Tytek Medical Inc Due to A defect involving an...
The Issue: A defect involving an occluded needle was discovered during a training exercise.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment...
The Issue: The AIA-2000 bar code scanners depend on the quiet zone to help identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Xtra Blood Glucose & Ketone Monitoring System Recalled by Abbott...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optium EZ Blood Glucose Monitoring System Recalled by Abbott Diabetes Care,...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Precision H Blood Glucose and Ketone Monitoring System Recalled by...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T....
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eleganza 5 (AC powered adjustable bed) Recalled by Linet Spol. S.r.o. Due to...
The Issue: A component used within the side rail mechanism may malfunction, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion...
The Issue: Sterile barrier system may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with...
The Issue: Nonfunctional key due to the potential for damage to the key pins cause by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST Recalled by...
The Issue: Components 2mm shorter than indicated on the package label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum MDS Screw 3.5x46mm ST Part Number: STRM-MDS-3546ST Recalled by...
The Issue: Components 2mm shorter than indicated on the package label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum MDS Screw 3.5x48mm ST Part Number: STRM-MDS-3548ST Recalled by...
The Issue: Components 2mm shorter than indicated on the package label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLASSIC Radiofrequency Cannula - Curved Recalled by Abbott Medical Due to A...
The Issue: A manufacturing error caused a single lot of 10mm active tip length Cannulas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.