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. 1,805 recalls have been distributed to Delaware in the last 12 months.
Showing 27161–27180 of 48,330 recalls
Recalled Item: Medline Incision and Drainage Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Staple Remover Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Incision & Drainage Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline CNTRL Line Removal Kit Scripps. Packaged in USA for Medline...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline CC Drawer 4 IV Circulation Pack Recalled by Medline Industries Inc...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Catheter Insertion Kit Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Circumcision Tray Kit Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Sheath Removal Kit Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinonide Gel USP Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Cross contamination with other products: traces of Dapsone were found in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: daVinci X EndoWrist(R) Stapler 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: Specific da Vinci Xi EndoWrist Stapler 45 instruments are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...
The Issue: Increased amount of residual blood present on the top of stopper well after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...
The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Death Wish Nitro Canned Cold Brew Coffee 11 oz Recalled by Death Wish Coffee...
The Issue: Potential for Clostridium Botulinum
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bio35 Recalled by Pro Bioteks Laboratories Due to Undeclared Soy
The Issue: Bio-35 has undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 Recalled by...
The Issue: Outer box fails to declare the allergen walnuts, the individual bar is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RHINO 7 Platinum 5000 Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PapaZen 3300 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.