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. 2,115 recalls have been distributed to Tennessee in the last 12 months.
Showing 3401–3420 of 52,000 recalls
Recalled Item: Azurion 5 M12 System Code: (1) 722227 (2) 722231 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monkey Spit "Atomic Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...
The Issue: Barbeque sauce product contains undeclared allergen listing of (Milk) in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monkey Spit "Swamp Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...
The Issue: Barbeque sauce product contains undeclared allergens (soy) contained in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by The Harvard Drug Group...
The Issue: CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monkey Spit "Monkey Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...
The Issue: Barbeque sauce product contains undeclared listing of (Milk) in product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL Recalled by Teva...
The Issue: Failed Stability Specifications - 12-month stability test result for one of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing device labeling is being updated to strengthen labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...
The Issue: Potential that the induction seal is not completely sealed to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...
The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Recalled by Nobel Biocare...
The Issue: Due to manufacturing issue (unintended by-product of the injection molding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger Recalled...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number:...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A820 myPTM Software Application associated with Medtronic SynchroMed Pump...
The Issue: Product complaints were received describing the A820 myPTM app taking longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a Recalled by...
The Issue: Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MSOT Acuity Echo is a Class 4 medical laser Recalled by Ithera Medical...
The Issue: The MSOT Acuity Echo does not include an adequate instruction for safe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Labeling...
The Issue: Labeling is insufficient regarding delays in access to medication. The firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK Recalled...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.