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. 1,747 recalls have been distributed to Delaware in the last 12 months.
Showing 34361–34380 of 48,330 recalls
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548470 (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: MM00548410 (XMD Recalled...
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: 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: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STD KIT GK260 Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.