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. 2,695 recalls have been distributed to Delaware in the last 12 months.
Showing 1061–1080 of 27,373 recalls
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuoDERM" Extra Thin dressings are highly flexible Recalled by ConvaTec, Inc...
The Issue: Wound dressing may have foreign matter on the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM Solution Set Recalled by Baxter Healthcare Corporation Due...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound...
The Issue: Production assembly error resulting in the potential for reversed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX...
The Issue: To provide further information to the user to ensure proper use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 88-Series Washer- Disinfector. Model Number: 88-5. Recalled by...
The Issue: Potential for device to overheat during operation if the circulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter....
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sharesource Connectivity Platform for Use with Homechoice Claria Product...
The Issue: Vantive has identified a software defect within the Sharesource Claria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mMR. Model Number: 10433372. Recalled by Siemens Medical Solutions...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Prisma. Model Number: 10849582. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.