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 20221–20240 of 27,373 recalls
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548680 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548950 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548650 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548830 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549570 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548850 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549390 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548560 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548920 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...
The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Recalled by Cardinal Scale Mfg Co Due to One complaint of a seat on...
The Issue: One complaint of a seat on a scale failing unexpectedly which can cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterGuard 5.5mm Econo Recalled by Ultradent Products, Inc. Due to Ultradent...
The Issue: Ultradent is recalling InterGuard 5.5mm Econo , lot#s BC2GN and BC4L7...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver¿ 518RX Vascular Stent with Rapid Exchange Delivery System Recalled by...
The Issue: Manufacturing of the joint between the inner catheter and stylet of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CA500 Epix Universal Clip Applier Product Usage: The Epix disposable...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STD GK258 Recalled by Applied Medical Resources Corp Due to Applied Medical...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbiq infusion pump is a device used in a Recalled by Hospira Inc. Due...
The Issue: Potential for the Symbiq pole clamp assemblies to be missing the rubber stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...
The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.