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. 2,603 recalls have been distributed to Tennessee in the last 12 months.
Showing 17441–17460 of 29,188 recalls
Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch...
The Issue: Hydrogel peeling from the pads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage:...
The Issue: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep...
The Issue: Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...
The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...
The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...
The Issue: One reported complaint and discovered that the outer vial was out of round...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...
The Issue: The label outside the cardboard box is labeled correctly but the pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by Medline Industries...
The Issue: Products labeled as sterile were distributed prior to sterilization
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER Recalled by Medline Industries...
The Issue: Products labeled as sterile were distributed prior to sterilization
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.