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. 997 recalls have been distributed to Delaware in the last 12 months.
Showing 17681–17700 of 48,330 recalls
Recalled Item: PC Application Software c4D as part of the device Catalyst: Recalled by...
The Issue: PC Application Software c4D not changing Site upon synchronization during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss Meditec AG VISUREF150 - Product Usage: Recalled by Carl Zeiss...
The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...
The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System. The EtCO2 module is a capnograph indicated for continuous...
The Issue: Infusion pump component defect may result in interruption of patient monitoring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...
The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to The...
The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System Recalled by CareFusion 303, Inc. Due to The Alaris PC unit...
The Issue: The Alaris PC unit can display incorrect syringe type and/or syringe sizes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to Tube trays may leak...
The Issue: Tube trays may leak which could invalidate patient results or assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY Recalled by...
The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine Recalled by...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Subpotent drug: Out of specification for assay at the 15-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Command Brands GelAnti Bac Instant Hand Sanitizer Recalled by ROQUE PLAST,...
The Issue: CGMP Deviation: Potential contamination with undeclared methanol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.