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. 997 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
997 in last 12 months

Showing 17781–17800 of 48,330 recalls

FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Chocolate Non-Dairy Frozen Dessert in pint sized Recalled...

The Issue: Undeclared cashews in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Vanilla Non-Dairy Frozen Dessert in pint sized Recalled by...

The Issue: Undeclared cashews in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint Recalled by...

The Issue: Undeclared cashews in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 10 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 2 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Subpotent Drug:...

The Issue: Subpotent Drug: Out-of-Specification potency results at the 30-day stability...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 28, 2020· Kader Exports Pvt. Ltd.

Recalled Item: Cooked Recalled by Kader Exports Pvt. Ltd. Due to Potential Salmonella...

The Issue: Frozen cooked shrimp is possibly contaminated with Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 28, 2020· Wright Medical Technology, Inc.

Recalled Item: Screw Removal Case Assembly Recalled by Wright Medical Technology, Inc. Due...

The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2020· Wright Medical Technology, Inc.

Recalled Item: Hardware removal kit Recalled by Wright Medical Technology, Inc. Due to...

The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit...

The Issue: Potential Endotoxin Contamination

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 40cc IAB Kit...

The Issue: Potential Endotoxin Contamination

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 40cc IAB...

The Issue: Potential Endotoxin Contamination

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 34cc IAB Kit...

The Issue: Potential Endotoxin Contamination

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible DCI Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 35cc IAB...

The Issue: Potential Endotoxin Contamination

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing