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 20621–20640 of 27,373 recalls
Recalled Item: Allura Xper FD20/15 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 Recalled by Philips Electronics North America Corporation Due to...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 15-12 (mono) Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS H3000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BN/BV3000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ FD Recalled by Philips Electronics North America Corporation Due to The...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 9 (biplane) Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BH5000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD 3.2 CLI DL380 Product Usage: MYLA is Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BH3000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLI V3.X TO V4.1 ML350 SERVER Product Usage: MYLA Recalled by...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA Recalled by...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by Philips Electronics North...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.