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 27601–27620 of 29,188 recalls
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For...
The Issue: The microelectrodes are not flush with the silastic substrate, may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Orthopedic Table Recalled by Mizuho OSI Due to Possible instability...
The Issue: Possible instability of Orthopedic Table Top. If the epoxy bond fails, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta Quadra Trial Broach size 0 part # 01.10.10.045 Recalled by Medacta...
The Issue: The tip of the Quadra Trial Broach size 0, broke during a surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Animas(R) 2020 Recalled by Animas Corporation Due to Due to an internal...
The Issue: Due to an internal calendar date limit (December 31, 2015) these pumps will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuietCare-Networked product Recalled by Intel-GE Care Innovations LLC Due to...
The Issue: Care Innovations detected a software anomaly: During the engineering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Non-DEHP Micro-Volume Extension Set Recalled by Baxter Healthcare...
The Issue: Some of the individual extension set packages were improperly sealed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Becton Recalled by Becton Dickinson & Co. Due to In-vitro diagnostic...
The Issue: In-vitro diagnostic reagents for microbiological testing may be reversed in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption...
The Issue: Some VITROS¿ Chemistry Products Vapor Adsorption Cartridge CAT No. 6800100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF Recalled by Philips Healthcare Inc. Due to Values of fluoroscopy...
The Issue: Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare...
The Issue: SR Instruments Inc. is implementing a field correction for the Joerns...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Medical Components, Inc dba MedComp Due to The affected product...
The Issue: The affected product was packaged with the incorrect introducer needle. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Laboratories Recalled by Abbott Laboratories Due to The Architect...
The Issue: The Architect 25-OH Vitamin D assay has the potential to generate falsely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device...
The Issue: Toshiba Medical Systems has received reports of startup issues with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(TM) Fildes Enrichment Recalled by Becton Dickinson & Co. Due to...
The Issue: Enrichment media intended to enhance the cultivation of various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flowtron Trio DVT Pump Recalled by Arjo, Inc. dba ArjoHuntleigh Due to The...
The Issue: The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...
The Issue: Firm has confirmed higher imprecision with the recalled lots on Beckman...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Standard Slingbar 450. The Standard Slingbar 450 is a Recalled by...
The Issue: Liko/Hill-Rom has received reports from facilities which indicate that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.