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. 1,856 recalls have been distributed to Delaware in the last 12 months.
Showing 16281–16300 of 48,330 recalls
Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...
The Issue: Teleflex is voluntarily recalling the products above due to customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methacholine Challenge 5-Syringe Test Kits Recalled by Edge Pharma, LLC Due...
The Issue: Temperature Abuse; labeled with the incorrect room temperature (15-25 ¿C)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 100mg Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quseo Fresco sold under the following brands and container sizes Recalled by...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Quesillo sold under the following brands and container sizes: El Recalled by...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Requeson/Ricotta Recalled by El Abuelito Cheese, Inc. Due to Potential...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...
The Issue: Discoloration and turbidity were present in the specified lots of STMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...
The Issue: Contact lenses may be mislabeled with the incorrect lens power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adam's Secret Extra Strength 1500 Recalled by Adams.Secret.co Due to...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adam's Secret Extra Strength 3000 Recalled by Adams.Secret.co Due to...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Chemical contamination; Unknown brown residue adhering to the inside of one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carestream Dental CS 3600 Single Use Normal Tips Recalled by CARESTREAM...
The Issue: The mirror may become detached and fall from the unit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE STRYDE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precice Bone Transport - Product Usage: intended for limb lengthening...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLEUR-EVAC Thoracic Catheters (CATHETER Recalled by TELEFLEX MEDICAL INC Due...
The Issue: Teleflex is recalling this product due to a lack of assurance of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.