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. 941 recalls have been distributed to Tennessee in the last 12 months.
Showing 45481–45500 of 52,000 recalls
Recalled Item: Kale Recalled by Plum Inc Due to Manufacturing defect leading to...
The Issue: Manufacturing defect leading to post-process contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum Kids Tropical Fruit Mashups Recalled by Plum Inc Due to Manufacturing...
The Issue: Manufacturing defect leading to post-process contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PACLITAXEL INJECTION Recalled by Fresenius Kabi USA, LLC Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert- Missing text on the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valacyclovir Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA,...
The Issue: Presence of Foreign Tablets/Capsules: Potential of Pravastatin tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB) Recalled by Arrow...
The Issue: Potential for a leak between the catheter and the bifurcate which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adipotrim XT Recalled by Deseo Rebajar Due to Undeclared Api
The Issue: Marketed Without an Approved NDA/ANDA: FDA lab results found undeclared API...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carisoprodol Tablets Recalled by West-Ward Pharmaceutical Corp. Due to...
The Issue: Presence of Foreign Substance; heavy metals (chromium, titanium etc) and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EOS System X- ray beam Digital radiography system used in Recalled by EOS...
The Issue: EOS imaging discovered during production internal testing that the X-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System is a pediatric and small stature...
The Issue: Part # 01-1008-0040/0047, ACL Sleeve Installation/ Insertion Tool, shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Optima XR220amx and Optima XR200amx with Digital Upgrade Mobile Recalled...
The Issue: There exists a software issue associated with patient selection from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teflon Tube Recalled by Stryker Howmedica Osteonics Corp. Due to Stryker...
The Issue: Stryker became aware during laboratory testing that there is a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho Molecular Products DigestzymeV. Dietary Supplement. Gastrointestinal...
The Issue: Ortho Molecular Products' vegetable enzyme vendor issued a recall of the raw...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Digestive enzyme capsules sold under the NOW Foods Recalled by NOW Foods Due...
The Issue: Digestive enzyme capsules manufactured by NOW Foods may contain the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Candela Laser GentleLase Pro Recalled by Candela Corporation Due to...
The Issue: Unintended single pulse maybe emitted to handpiece prior to pressing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axillent Debakey Grasping Forceps Recalled by Karl Storz Endoscopy America...
The Issue: KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrument Manager driver : Driver sysu100i that connects to the Recalled by...
The Issue: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Chemistry Systems models 1200 Recalled by Siemens Healthcare...
The Issue: The ADVIA Chemistry software systems using certain software versions allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems FOL Folic Acid Recalled by Siemens Healthcare...
The Issue: potential for an accelerated decline in counts per second (CPS) for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imitrex STATdose System Recalled by GlaxoSmithKline, LLC. Due to Lack of...
The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Actavis Elizabeth LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: During routine stability testing one tablet was found with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.