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. 2,595 recalls have been distributed to Delaware in the last 12 months.
Showing 14201–14220 of 27,373 recalls
Recalled Item: Achieva 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR-OR 1.5T Recalled by Philips Medical Systems Nederlands Due to There is a...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T for PET Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama 1.0T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 0.5T Standard Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T High Performance Recalled by Philips Medical Systems Nederlands...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The WinStation Retinal Imager Recalled by Merge Healthcare, Inc. Due to...
The Issue: Certain configurations of Merge Eye Station hardware may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...
The Issue: When switching back & forth between multiple UV instances in the Windows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...
The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...
The Issue: The kits may contain the incorrect number of components or the kits may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...
The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.