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. 1,110 recalls have been distributed to Tennessee in the last 12 months.
Showing 6361–6380 of 52,000 recalls
Recalled Item: 20" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) GYN CDS Recalled by...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) TURNOVER KIT Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactated Ringer's Injection USP Recalled by B. Braun Medical Inc Due to Lack...
The Issue: Lack of assurance of sterility: bags have the potential to leak..
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Citrate 2 Recalled by IntegraDose Compounding Services LLC Due to...
The Issue: Lack of Assurance of Sterility: leaking bags
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Oral Solution Recalled by Amneal...
The Issue: Superpotent Drug: Due to overfilling of drug powder
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VCF Vaginal Contraceptive Film (nonoxynol-9 Recalled by Apothecus...
The Issue: cGMP Diviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models:...
The Issue: Coolant level in the cooling circuit drops below a certain level, this may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24K Premium Lense Recalled by Ontact Inc Due to Contact lenses recalled due...
The Issue: Contact lenses recalled due to potential bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Surgical Tape Recalled by 3M Company - Health Care Business Due...
The Issue: Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.