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 28521–28540 of 52,000 recalls
Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...
The Issue: Stent length on the label may not match the length of the stent itself.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...
The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASTERA Multifocal Toric Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 38 Sphere Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...
The Issue: The firm received reports of two breakages of the pin tips which occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epi proColon Plasma Quick Kit Recalled by Epigenomics Ag Due to The...
The Issue: The diagnostic test kit may produce invalid test runs which may delay test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoBase Succinylacetone Assay Solution Recalled by PerkinElmer Life and...
The Issue: There is a potential for leaking vials for certain lot numbers where, if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM0405 Mueller-Hinton Broth IVD Recalled by Remel Inc Due to Product may...
The Issue: Product may have incorrect cation information detailed on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE(TM) BRAND Recalled by 3M Company - Health Care Business Due to Mold was...
The Issue: Mold was found on the non-patient contact surfaces of the product and was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.