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

48,330 total recalls
907 in last 12 months

Showing 43621–43640 of 48,330 recalls

Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: B-50 capsules Recalled by Mira Health Products Ltd. Due to Marketed without...

The Issue: Marketed without an Approved NDA/ANDA; product found to contain methasterone...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 22, 2013· Torrent Pharma Inc

Recalled Item: Olanzapine Tablets Recalled by Torrent Pharma Inc Due to Defective...

The Issue: Defective Container; This action is being taken as a precautionary measure...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: METHA-DROL Extreme capsules Recalled by Mira Health Products Ltd. Due to...

The Issue: Marketed without an Approved NDA/ANDA; product found to contain dimethazine...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: Super-DMZ Rx 2.0 Capsules Recalled by Mira Health Products Ltd. Due to...

The Issue: Marketed without an Approved NDA/ANDA; product contains the steroid...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 22, 2013· MCKESSON TECHNOLOGIES INC

Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...

The Issue: The firm issued a clinical alert after users reported an issue where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR V-Patch Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR TacShield Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 300 and ACL TOP 300 CTS (Japan) Recalled by Instrumentation...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Blue Belt Technologies MN

Recalled Item: Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue...

The Issue: Blue Belt Technologies is recalling sterile Monitor Drapes used with their...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
FoodJuly 19, 2013· Plum Inc

Recalled Item: Plum Organics Mighty 4 Essential nutrition blend Recalled by Plum Inc Due to...

The Issue: Intermittent ineffective hermetic seal on pouch package leading to potential...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2013· Plum Inc

Recalled Item: Plum Organics Mighty 4 Essential nutrition blend Recalled by Plum Inc Due to...

The Issue: Intermittent ineffective hermetic seal on pouch package leading to potential...

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

Class II — Potential Health HazardOngoing
Refund