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 26221–26240 of 27,373 recalls
Recalled Item: ABX PENTRA ML Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX PENTRA ML because they have confirmed an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...
The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...
The Issue: The Back Table Cover component in the custom pack was placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Flow Module indicated for use Recalled by...
The Issue: Terumo Cardiovascular Systems (CVS) received one report of a flow module for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...
The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helion and Xenion surgical lights Recalled by Trumpf Medical Systems, Inc....
The Issue: Incidents regarding fractures of the front joint of the spring arm have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Mast Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Male Recalled by Cure Medical LLC Due to The firm initiated the product...
The Issue: The firm initiated the product recall because labeling on some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Mast Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Single Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Double Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin C5 Perfusion System Recalled by Sorin Group USA, Inc. Due to Sorin...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...
The Issue: A patient was seriously mistreated after a user made and saved an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...
The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iris Diagnostics Division iQ Control/Focus Set Recalled by Iris Diagnostics...
The Issue: The firm initiated this recall because complaints from customers reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.