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. 2,637 recalls have been distributed to Tennessee in the last 12 months.
Showing 14981–15000 of 29,188 recalls
Recalled Item: Epix Electrosurgical Probes with Smoke Evacuation Recalled by Applied...
The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GelPOINT Path Transanal Procedural Pack with Epix Electrosurgical L-Hook...
The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended...
The Issue: Potential for the software on Automated PD System cyclers which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIA Automated Peritoneal Dialysis System Product Usage: It is intended...
The Issue: Potential for the software on Automated PD System cyclers which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic...
The Issue: Negative bias results when using VITROS VALP Reagent, GEN 25.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 1-2 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement...
The Issue: Product mix up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius Knee Cemented Tibial Component Product Usage: Knee replacement...
The Issue: Product mix up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProSun V3 42 Xlc(160w)(10 minutes) tanning bed Recalled by ProSun...
The Issue: ProSun International LLC discovered discrepancies in their Quality Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed Recalled by ProSun...
The Issue: ProSun International LLC discovered discrepancies in their Quality Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 5-6 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 7-8 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROXIMATE¿ HCS Hemorrhoidal Circular Stapler Product Code: PPH01 PPH01: The...
The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK STEM with Microporous Surface MP Reconstruction Prosthesis Recalled by...
The Issue: The reaming guide and the guide rod can't be screwed into the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.