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. 2,674 recalls have been distributed to Delaware in the last 12 months.
Showing 4481–4500 of 27,373 recalls
Recalled Item: Peel-Away Introducer - Intended for the percutaneous introduction of balloon...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Trumpet Needle Guide ring can detach when excessive pressure is applied.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Intended to be used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator With AQ Hydrophilic Coating - Intended to be used Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs...
The Issue: Potential for positively biased results due to signal reduction over shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Coons Taper - Used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chiba Biopsy Needle - Used for aspiration biopsy. PART Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete Recalled...
The Issue: The reason for the recall is the pneumatic tubing used in the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix Yeast ID Panel is a self-inoculating (when used Recalled by...
The Issue: Esculin, a substrate used in other panels and normally in A16 well, was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix NMIC-306 Panel is a self-inoculating (when used with Recalled by...
The Issue: Products were found to have confirmed drug cross contamination prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Structural Balloon Trocar Recalled by Covidien, LP Due...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareEvent Event Management System Recalled by Philips North America Due to...
The Issue: It was found that the Care Assist mobile application (version 4.1.1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.