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. 1,069 recalls have been distributed to Delaware in the last 12 months.
Showing 6721–6740 of 48,330 recalls
Recalled Item: W&H Surgical handpiece S-12. For Surgical treatment of dental hard Recalled...
The Issue: 1:2 speed increasing surgical handpieces have been incorrectly laser marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Gastric-Jejunal Feeding Tube Recalled by Avanos Medical, Inc. Due to...
The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC*...
The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IV Start Kit Recalled by Medical Action Industries, Inc. 306 Due to The kits...
The Issue: The kits contain saline flush syringes which were recalled by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Amneal Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ready To Bake Chocolate and Almond Variety Pk () Recalled by Wegmans Food...
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 5 oz 2pk Chocolate Croissant Recalled by Wegmans Food Markets, Inc. Due to...
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ready To Bake Double Chocolate Croissant () Recalled by Wegmans Food...
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 9 oz 10pk Assorted Mini Danish Recalled by Wegmans Food Markets, Inc. Due to...
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 24ct Petite Pastry Tray Recalled by Wegmans Food Markets, Inc. Due to...
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vasostrict (vasopressin in 5% Dextrose) Injection Recalled by Par Sterile...
The Issue: Superpotent Drug: Assay from the 3-month and 6-month stability intervals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules USP Recalled by Amerisource Health Services LLC Due to...
The Issue: Failed Impurities/Degradation Specification.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.