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. 2,495 recalls have been distributed to Delaware in the last 12 months.
Showing 19581–19600 of 27,373 recalls
Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...
The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...
The Issue: Incorrect expiration date was printed on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...
The Issue: Incorrect expiration date was listed on the label. Correct expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...
The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.