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. 2,664 recalls have been distributed to Tennessee in the last 12 months.
Showing 10561–10580 of 29,188 recalls
Recalled Item: Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN Recalled by Combat...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Hypodermic Syringe 10 ml Recalled by Becton Dickinson & Company Due to...
The Issue: The product packaging for the 10 ml eccentric tip syringe may exhibit open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution: The IACS is Recalled...
The Issue: The Infinity M540 patient monitor may randomly reboot due to an error to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. Clavicle Plating System Recalled by Biomet, Inc. Due to The...
The Issue: The instruments may become cold welded together when the drill is inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EOSedge system may acquire two simultaneous orthogonal planar images...
The Issue: Inadequate images resizing and 2D measurement errors may occur when biplanar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used Recalled by...
The Issue: FUJIFILM has become aware that incorrect concentration values were printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott i-STAT CG8+ cartridges - IVD Intended for quantitative measurement...
The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott i-STAT EG7+ cartridge-IVD. Intended for the quantitative measurement...
The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge CM320 Series Washer Disinfector - Product Usage: A multi Recalled by...
The Issue: The potential that the plastic inlet hose connections may deform or break as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set Recalled by...
The Issue: There were customer reports of separation between the tubing and Male Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brain Heart Infusion Agar with 6 ug/ml Vancomycin Cat no: Recalled by Hardy...
The Issue: Complaints were received reporting of Staphylococcus aureus (ATCC 29213)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No....
The Issue: Medical device non-conformance to electrical safety standard (IEC 60601-1).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Acapella DH Vibratory PEP Device - Product Usage: a Recalled by...
The Issue: Shipping box may contain wrong model.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...
The Issue: Misleading error messages and a gap in the Operator Manual which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...
The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSABOND AB 40 GRAMS FORMULATION 2 Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential heat and humidity exposure. The affected lot contained an atypical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...
The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit (LCSU 4) Recalled by Laerdal Medical (Suzhou)...
The Issue: Component failures may cause the unit to lose all suction. Users will need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnshLabs - SARS-CoV2 IgM ELISA (u-Capture) Recalled by Ansh Labs, LLC Due to...
The Issue: Labeling update; To reduce the risk of false positive/false negative results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.