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 27061–27080 of 27,373 recalls
Recalled Item: KRD1 PedFuse Rods Recalled by SpineFrontier, Inc. Due to One of the rods in...
The Issue: One of the rods in each of two test constructs did not meet fatigue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker Orthopaedics has become aware of the potential for cracking of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Accolade Offset Rasp Handle Howmedica Osteonics...
The Issue: Stryker Orthopaedics has become aware of the potential for the above noted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineFrontier S-Lift Lock Shaft Inserter Recalled by SpineFrontier, Inc. Due...
The Issue: It has been verified through field use that there are two possible breakages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3100 Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3100-IQ Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100 IQ Recalled by GE Healthcare, LLC Due to While...
The Issue: While performing a fluoroscopic examination on the GE Innova systems, there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3131-IQ Mobile X-ray system. The innova systems...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Eon Mini Neurostimulation (IPG) System (Model 3788) is a 16-channel...
The Issue: As of 11/30/2011, St. Jude Medical has received 110 patient complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon (Model 3716) IPG is a dual channel Recalled by Advanced Neuromodulation...
The Issue: As of 11/30/2011, St. Jude Medical has received 110 patient complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini Neurostimulation (IPG) System (Model 3788) Recalled by Advanced...
The Issue: The firm has received 112 complaints of the Eon Mini IPGs that lost the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron Systems Synchron Calibrator Multi Calibrator Diskettes Recalled by...
The Issue: The recall was initiated because Beckman Coulter has confirmed a mislabeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Stainer Floor Cabinet Recalled by Beckman...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the DxH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Instrument System Recalled by Beckman Coulter...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the DxH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vector TAS Modular Driver Recalled by Ormco/Sybronendo Due to The...
The Issue: The Instructions For Use (IFUs) for Vector TAS Modular Driver for some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm)...
The Issue: Some of the sterile packages had broken seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a Recalled by Tripath...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Upgrade Kit: 1.3.0.3/1.2 DiTi Cone. The PrepStain System is...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain PM Kit Recalled by Tripath Imaging, Inc. Due to Some Prep Stain...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Slide Processor. The PrepStain System is a liquid-based thin...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.