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. 2,469 recalls have been distributed to Delaware in the last 12 months.
Showing 24061–24080 of 27,373 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Camino Advanced Monitor with Waveform Display Model CAM01 Integra...
The Issue: Integra became aware through a complaint from a single non-US customer that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: outer box: Recalled by Biomet, Inc. Due to Inner label of PN: 906768 Lot:...
The Issue: Inner label of PN: 906768 Lot: 055450 CurvTek Eye Needle 22mm X-Large states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaTrak¿ 3500 Plus Recalled by GE OEC Medical Systems, Inc Due to GE OEC...
The Issue: GE OEC Medical Systems Inc is recalling InstaTrak¿ 3500 Plus, ENTrakTM Plus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000 Recalled by Biomet,...
The Issue: Investigation identified that the outer label, inner label, and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 Med/Surg Bed Secure II and the 3002 S3 are Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Firebird Spinal Fixation System Instrumentation Modular Screw...
The Issue: Orthofix received 6 complaints which resulted in a reportable events due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Secure II Med/Surg Bed Secure II and the 3002 S3 Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Interlink threaded lock cannula This is a locking blunt Recalled by...
The Issue: BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HT Connect Peripheral Guide Wire Part Number Description 1012587 018...
The Issue: Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RTP System. Used to create treatment plans for any Recalled by Elekta,...
The Issue: When bolus is present, the Effective Depth (with bolus) to the weight point...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI The Elekta Synergy S is intended to be Recalled by Elekta, Inc....
The Issue: Potential collision risk when using XVI and external beam shaping devices.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port Kit with Access Infusion Set under the following labels: Recalled by...
The Issue: Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with FF WS These products are permanently installed diagnostic...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity. Version 1.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.0 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...
The Issue: XVI can incorrectly calculate the target position of the treatment table.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.