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. 1,824 recalls have been distributed to Delaware in the last 12 months.
Showing 22721–22740 of 48,330 recalls
Recalled Item: Mirapex (pramipexole dihydrochloride) Tablets Recalled by Boehringer...
The Issue: Failed Tablet/Capsule Specifications: identification of low weight tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Remedies New Baby Essentials Kit. Each kit contains 1 Recalled by...
The Issue: Incorrect/undeclared excipients: Kit carton bear incorrect labeling for two...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PL Trader Joe Natural Creamer - Vanilla 12/32oz Recalled by GOOD KARMA FOODS...
The Issue: Product was recalled due to undeclared milk. The Contains statement does not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to Potential...
The Issue: Increased risk of false positive Enterobacteriaceae and Escherichia coli...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valsartan Tablets USP 160 mg Recalled by American Health Packaging Due to...
The Issue: CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docetaxel Injection USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Defective Container: complaint for seal and cap vial issues that could lead...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...
The Issue: Elevated rates of false positive results for Campylobacter and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...
The Issue: When a patient is selected in the patient data and another patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBeam Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to...
The Issue: Certain lots may develop an internal leak due to a micro-crack in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEOPARD Miracle Honey packaged in a wooden box Recalled by USA LESS Inc. Due...
The Issue: Marketed Without An Approved NDA/ANDA: product tainted with undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....
The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 50 mg 50 Tablets (5x10) Unit Dose boxes...
The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....
The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled...
The Issue: Based on internal investigations, Fresenius Kabi has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan) Recalled by Petra...
The Issue: Does Not Meet Monograph: product contains, triclosan, an ingredient that can...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aspirin and Extended-release Dipyridamole Capsules Recalled by American...
The Issue: Failed Impurities/Degradation Specifications; out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablets USP 10 mg Recalled by AVKARE...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.