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. 2,699 recalls have been distributed to Delaware in the last 12 months.
Showing 241–260 of 48,330 recalls
Recalled Item: Medline Convenience Kits: 1) KIT UROLOGY SLING Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) SPINAL CDS Recalled by Medline Industries, LP...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Surgical Drapes: 1) SHEET Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) CHEST/BREAST-LF Recalled by Medline Industries,...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) DRAPE PACK Recalled by Medline Industries, LP...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) SCC RF PAIN MGMT Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips North America Llc Due to As part of the...
The Issue: As part of the CT systems sub assembly, thirty-two (32) fasteners are used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT Recalled by Philips North America Llc Due to As part of the CT...
The Issue: As part of the CT systems sub assembly, thirty-two (32) fasteners are used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT Recalled by Philips North America Llc Due to As part of the...
The Issue: As part of the CT systems sub assembly, thirty-two (32) fasteners are used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 on Rails Recalled by Philips North America Llc Due to As...
The Issue: As part of the CT systems sub assembly, thirty-two (32) fasteners are used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.