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 26481–26500 of 27,373 recalls
Recalled Item: The Bio-Rad MONOLISA Anti-HBs EIA is for In Vitro Diagnostic Recalled by...
The Issue: Prolonged exposure of the MONOLISA Anti-HBs EIA Conjugate Diluent component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Cardiovascular (CV) Reporting Reporting tool used for structured...
The Issue: Content entered into the "Conclusions" free text box on the Report Writer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TxRx Knee 15 Coil 3T. For use in conjunction with Recalled by Quality...
The Issue: On July 27, 2012, it was reported to the firm that the Siemens 3T 15ch Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interface module for CDl System 100/101 Product Usage: The Interface...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Styker Orthobiologics Vita Plasma Separator Recalled by Stryker...
The Issue: When preparing plasma using VitaPrep, it was reported that a small amount of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini - 3788 (IPG) Recalled by St. Jude Medical Due to As part of St....
The Issue: As part of St. Jude Medical's routine tracking and product monitoring, they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St....
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...
The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...
The Issue: There is a possibility that the screw channel that holds the rod in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...
The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.