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. 2,678 recalls have been distributed to Delaware in the last 12 months.
Showing 4361–4380 of 48,330 recalls
Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...
The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atovaquone Oral Suspension Recalled by Bionpharma Inc. Due to Microbial...
The Issue: Microbial Contamination of a Non-sterile Product: The product was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The IMAGEnet 6 Ophthalmic Data System is a software program Recalled by...
The Issue: The overlay of visual field test locations on a probability map, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use...
The Issue: A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing...
The Issue: The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.M. Recalled by AbbVie Inc. Due to Lack of Assurance of Sterility: The...
The Issue: Lack of Assurance of Sterility: The impacted lots may contain a breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACRI-LUBE Recalled by AbbVie Inc. Due to Lack of Assurance of Sterility:...
The Issue: Lack of Assurance of Sterility: The impacted lots may contain a breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambu¿ VivaSight 2 DLT Endobronchial tube Recalled by Ambu Inc. Due to Ambu...
The Issue: Ambu has received complaints on Ambu¿ VivaSight 2 DLTs regarding hyper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Cystoscope Outer Sheath Recalled by Olympus Corporation of the...
The Issue: Product being removed due to incompatibility when used in conjunction with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S'mores Bites Recalled by Nuts.com Due to Undeclared Allergen
The Issue: Undeclared Allergen, milk - a mix-up between the product description and the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog...
The Issue: Olympus is removing the statement of compatibility with a GreenLight Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon- Indicated for use in adult and Recalled by...
The Issue: Mislabeled Glo Cath Label (attached to the device) states: 11 mm, 12 mm, 13...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing...
The Issue: There is a potential for pinholes in the applicator pouch film which creates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Infusion System Recalled by Zyno Medical LLC Due to There is a defect...
The Issue: There is a defect in the air-in-line software algorithm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity m HPV AMP Kit Recalled by Abbott Molecular, Inc. Due to...
The Issue: Abbott has identified an increase of incidences regarding Error Code (EC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity m STI AMP Kit Recalled by Abbott Molecular, Inc. Due to...
The Issue: Abbott has identified an increase of incidences regarding Error Code (EC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Life2000 Ventilation System Recalled by Baxter Healthcare...
The Issue: The Life2000 ventilator may fail to initiate the Low Gas Pressure alarm if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Informatics Solution with software versions: 4.20 Recalled by...
The Issue: Synapsys software versions 4.20, 4.30, 5.10, 5.20, or 5.30 and utilizing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Aid Antiseptic Ointment Recalled by Zhejiang Jingwei Pharmaceutical...
The Issue: Incorrect/Undeclared Excipients: The inactive ingredients labeled on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: UroPass Ureteral Access Sheaths Product Name: Ureteral Access...
The Issue: Exposure of the UroPass product to Ultraviolet ( UV ) Radiation can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.