Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,017 recalls have been distributed to Delaware in the last 12 months.
Showing 16661–16680 of 48,330 recalls
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: 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: 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: Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Recalled by...
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: Oxycodone Hydrochloride Oral Solution Recalled by Genus Lifesciences Inc....
The Issue: Presence of Foreign Substance: Particulate matter was found in multiple lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...
The Issue: CGMP Deviations: product manufactured at the same facility that produced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...
The Issue: CGMP Deviations: product manufactured at the same facility that produced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...
The Issue: CGMP Deviations: product manufactured at the same facility that produced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or 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 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: 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: 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: 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: 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: 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: 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: Zerbaxa (ceftolozane and tazobactam) 1.5g per vial for injection Recalled by...
The Issue: Lack of assurance of sterility: The results of sterility tests of seven...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benzhydrocodone and Acetaminophen Tablets Recalled by KVK-Tech, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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.