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. 2,699 recalls have been distributed to Delaware in the last 12 months.
Showing 301–320 of 48,330 recalls
Recalled Item: Lanreotide Injection Recalled by Cipla USA, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. Recalled by AVID Medical,...
The Issue: Tyvek bag seal issue which may compromise sterility of the kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioGlo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bio Glo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Tears Polyethylene Glycol 400 0.4% w/v Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Gel Hypromellose USP 0.3% w/v Recalled by Wizcure Pharmaa Private...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Gonio Eye Lubricant Recalled by Wizcure Pharmaa Private Limited Due to...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Recalled by...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHNaO Fluorescein Sodium Ophthalmic Strips Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Alvogen, Inc Due to Product Mix-Up:...
The Issue: Product Mix-Up: A single bottle of this lot was reported by a pharmacy to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rosuvastatin Tablets Recalled by AvKARE Due to Out of specification for...
The Issue: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET...
The Issue: Under circumstances involving exposure to particular chemicals and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number:...
The Issue: Products were mislabeled as the 6mm product but included the 5 mm product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEAR Implant. Model Number: 1000. Recalled by Miach Orthopaedics Due to...
The Issue: Incorrect expiration date on label that extends beyond the product's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Icosapent Ethyl capsules Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Subpotent Drug: Due oxidation caused by leakage of the contents of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinolone Acetonide Solution Topical Solution USP Recalled by SUN...
The Issue: Failed Impurities/Degradation Specifications: Out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ondansetron Orally Disintegrating Tablets Recalled by Glenmark...
The Issue: Defective container: Preferred Pharmaceuticals received a letter from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: da Vinci 5 Surgeon Console Viewer Display Recalled by Intuitive Surgical,...
The Issue: Robotic-assisted surgical system has Viewer Display manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.