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 24301–24320 of 27,373 recalls
Recalled Item: 15 L Cycler Drainage Bag Product Usage: For use with Recalled by Baxter...
The Issue: The large tube clamp used to close the drain tube on the 15 L Cycler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biotene Moisturizing Mouth Spray Recalled by GlaxoSmithKline, LLC. Due to...
The Issue: Label indicates, "Sweetened with xylitol and Sorbitol", however product does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System Recalled by Philips Medical Systems North America...
The Issue: A problem has been detected with Philips Model EPIQ 7 Ultrasound System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch &...
The Issue: Lens was manufactured with incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cutera brand truSculpt infrared System (optional) Recalled by Cutera, Inc....
The Issue: Cutera received two adverse events associated with the edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...
The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...
The Issue: One material batch used for production of the affected parts of the Synthes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...
The Issue: Labeling inconsistency
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...
The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...
The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...
The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEXGEN MIS TIBIA PLATE PR NEXGEN TAPER PLUG NEXGEN PRECOAT Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...
The Issue: If the couch, with the footrest extension attached, is positioned where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System Recalled by...
The Issue: Incorrect instructions for use (IFU).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.