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 26181–26200 of 27,373 recalls
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake...
The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Cellestis 1 ml QuantiFERON¿ - TB ANTIGEN Recalled by Cellestis Inc...
The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeGotzen XRay unit XGenus Dental X-ray unit. Recalled by DeGotzen Due to It...
The Issue: It was discovered at the WEAC Labs method sample did not meet requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Definium 5000/5220493-2 X-Ray System Recalled by GE...
The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Definium 5000 / 5220493 X-Ray System Recalled by GE...
The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***This recall is being conducted due to an incomplete recall Recalled by...
The Issue: This recall is the same issue for the FDA processed recall initiated by Moog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hem-o-lok Large Polymer Ligating Clips Recalled by Teleflex Medical Due to...
The Issue: Product is being recalled due to the possibility that the tray may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Belmont Rapid Infuser Recalled by Belmont Instrument Corporation Due to Leak...
The Issue: Leak from a saline bag caused saline to drip along the back of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (l) Visum Halogen Surgical Light Recalled by Stryker Communications, Inc....
The Issue: Stryker has become aware that there is a low likelihood of incomplete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ILLlCO¿ MIS Posterior Fixation System Recalled by Alphatec Spine, Inc. Due...
The Issue: The firm initiated the recall because the stainless steel guide-wire of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.