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 28501–28520 of 29,188 recalls
Recalled Item: ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with Recalled by Sendx...
The Issue: The firm recalled because the glucose measurements from a patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The Tyvek pouch...
The Issue: The Tyvek pouch label for this device states: 'with holster'; however, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The carton label for...
The Issue: The carton label for this device has the manufacturer symbol where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathFinder NXT Pivoting Percutaneous Rod Holder This device is an Recalled...
The Issue: Complaints have been reported where, during surgery, the surgeon was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap(R) - Miethke Shunt System Recalled by Aesculap, Inc. Due to The...
The Issue: The deflector may not move freely on the ventricular catheter. The deflector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M525 F50 Surgical Microscope Recalled by Leica Microsystems, Inc. Due...
The Issue: Leica Microsystems evaluated data showing that a malfunction resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...
The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4-Hytrel Zipper Toga Product Usage - The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...
The Issue: The recall was initiated because Advanced Sterilization Products has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips Recalled by PSC Industries Inc...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that the outer carton label of this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...
The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.