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. 2,457 recalls have been distributed to Delaware in the last 12 months.
Showing 26121–26140 of 27,373 recalls
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge.115mmx115mm Pledget Recalled...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem Recalled by Stryker...
The Issue: Stryker has received a report that single size 3.5 stem was packaged as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Siemens Symbia S series is intended to aid in detecting Recalled by...
The Issue: There is a potential for the linear bearing car to fail allowing the ball...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Siemens Symbia T series is intended to aid in detecting Recalled by...
The Issue: There is a potential for the linear bearing car to fail allowing the ball...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Multianalyte Control Recalled by Alere San Diego, Inc....
The Issue: Out of range (increased) HDL Cholesterol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Calibration Verification Recalled by Alere San Diego,...
The Issue: Out of range (increased) HDL Cholesterol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Taxo XV Factor Strips Recalled by Becton Dickinson & Co. Due to In...
The Issue: In vitro diagnostic test kit was not manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard...
The Issue: Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriVascular brand Fill Polymer Kit Recalled by Trivascular, Inc Due to...
The Issue: Selected lots of the Fill Polymer Kit (European Model Number: TVFP14- B) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling Recalled by...
The Issue: American Medical Systems¿ (AMS) is issuing a voluntary recall on a number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00)...
The Issue: IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...
The Issue: Complaint received from sales representative that the drill guide tubes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Sliced CT Scanner System Recalled by Philips And Neusoft...
The Issue: The four screws that secure the patient table top to the carrier pulled out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...
The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.