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. 1,830 recalls have been distributed to Delaware in the last 12 months.
Showing 18281–18300 of 48,330 recalls
Recalled Item: Goodness Gurus Recalled by MICHIGAN HERBAL REMEDIES Due to Undeclared Lead
The Issue: Chemical contamination: product contains elevated levels of undeclared lead.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tasty Drops Recalled by MICHIGAN HERBAL REMEDIES Due to Undeclared Lead
The Issue: Chemical contamination: product contains elevated levels of undeclared lead.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gordon Choice Imitation Crab Supreme Style Recalled by Trident Seafoods...
The Issue: Product may contain undeclared egg white.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chembio DPP¿ Micro Reader for use with the DPP¿ COVID-19 Recalled by Chembio...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chembio DPP COVID-19 IgM/IgG System- Rrapid immunochromatographic test for...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chembio DPP¿ Micro Reader II for use with the DPP¿ Recalled by Chembio...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anjon Bremer Molded Crown. bone fixation fastener for spinal use. Recalled...
The Issue: High rate of galling of one threaded component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal Recalled by...
The Issue: Removal for a specific lot, lot number 70128207, of Holder HKHZ 19 for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brill 30 lb. cases of 480 1.0 oz. chocolate chip Recalled by Brill Inc Due...
The Issue: Products may contain undeclared walnuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DxA 5000 Recalled by Beckman Coulter Biomedical GmbH Due to The DxA 5000...
The Issue: The DxA 5000 instructions for use may be confusing regarding the re-use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Migrating Indicator Recalled by Resource Optimization & Innovation...
The Issue: The firm received reports from customer that the Regard Migrating Indicator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Recalled by FHC,...
The Issue: An electrical sub-circuit was not properly connected. Its purpose is to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Childrens Dimetapp Cold & Cough Recalled by Glaxosmithkline Consumer...
The Issue: Defective Delivery System: the dosing cups are missing graduations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Childrens Robitussin Honey Cough and Chest Congestion DM Recalled by...
The Issue: Defective Delivery System: the dosing cups are missing graduations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay: Luminex Recalled by Luminex Corporation...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Recalled by...
The Issue: Convenience kit mislabeled with the incorrect catheter effective length on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...
The Issue: Superpotent Drug: The beginning portion of the batch appears to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...
The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.