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. 986 recalls have been distributed to Tennessee in the last 12 months.
Showing 38081–38100 of 52,000 recalls
Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...
The Issue: Complaints that the femoral head could not be assembled with its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Family Gourmet Natural Whole Grain Brown Rice Recalled by Family Dollar...
The Issue: Live insects were noted inside several unopened bags of product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Family Gourmet Long Grain Enriched White Rice Recalled by Family Dollar...
The Issue: Live insects were noted inside several unopened bags of product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3-Day Cleanse Recalled by TN Juice Bar Due to Unpasteurized juice product...
The Issue: Unpasteurized juice product with elevated pH levels and unlabeled almond...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fenoglide (fenofibrate) tablets Recalled by Valeant Pharmaceuticals North...
The Issue: Failed Dissolution Specifications: Failed 24 month dissolution testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...
The Issue: This product was produced using a finishing process not identified as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Pipeline Embolization Device -Pipeline Flex Embolization Device The...
The Issue: The firm is recalling Pipeline and Pipeline Flex Embolization Devices from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...
The Issue: There is a defect in one lot of a buffer, non-specific background staining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Recalled...
The Issue: Chemical Contamination: Naphthalene compound identified in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: French Burnt Peanuts Recalled by Old Time Candy Due to The firm has the...
The Issue: The firm has the incorrect ingredient statement on the package. The...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....
The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inserter for Titanium Elastic Nails (TEN) Recalled by Synthes (USA) Products...
The Issue: potential for mechanical failures such as breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 123 POC system The cobas b 123 POC Recalled by Roche Diagnostics...
The Issue: under specific settings, an issue may occur during simultaneous Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer...
The Issue: In about 5% of tested samples, the outer tray was found to be compromised....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...
The Issue: The firm determined that 25 lots had been manufactured with a minor surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...
The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCG 3000 Units/mL Injection Recalled by Kalman Health & Wellness, Inc. dba...
The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 17-Alpha Hydroxyprogesterone 250 mg/mL in Sesame Oil Injection Recalled by...
The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 10 Recalled by Kalman Health & Wellness, Inc. dba Essential Wellness...
The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.