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. 2,509 recalls have been distributed to Tennessee in the last 12 months.
Showing 24541–24560 of 29,188 recalls
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a...
The Issue: In the case of a loss of GUI display due to a Backlight Inverter PCBA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch Critical Care Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has received complaints from the field alleging instances where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 It is intended to be used Recalled by Zimmer...
The Issue: Software corrections reactivating the cooperative endoscopy mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System...
The Issue: Covidien is conducting a medical device field correction for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eye-pak 7407 Tray Support Cover Recalled by Alcon Research, Ltd. Due to The...
The Issue: The peel pouches of the Tray Support Covers may be insufficiently sealed so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 300 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM DISTAL TAPERED Distal Stem Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM DISTAL TAPERED Recalled by DePuy Orthopaedics, Inc. Due to The...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Recalled...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.