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. 2,636 recalls have been distributed to Tennessee in the last 12 months.
Showing 15461–15480 of 29,188 recalls
Recalled Item: Gibco GlutaMAX Supplement Recalled by Life Technologies, Corp. Due to Leaky...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco DPBS Recalled by Life Technologies, Corp. Due to Leaky bottles due to...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Sodium Pyruvate (100 mM) SKU 11360070 Recalled by Life Technologies,...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant...
The Issue: RTInterface error in the event of an I/O error between the IGC PCB and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2 Recalled by...
The Issue: Defect consists of a small crack in the top end of the barrel near the needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...
The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...
The Issue: One lot of the specified needles is not performing as intended due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...
The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 12mm SpinDown Clamp Recalled by Zimmer...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon Natura Model 210-005-152 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-005-152 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon Natura Model 210-105-251 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-005-153 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-105-151 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-005-151 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.