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 5101–5120 of 27,373 recalls
Recalled Item: AirTouch N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirTouch F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protege GPS Self-Expanding Peripheral Stent System Recalled by Medtronic...
The Issue: Seal defects could compromise the ability of the product packaging to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F30i Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F30 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...
The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica HistoCore PEGASUS (PROCESSOR Recalled by LEICA BIOSYSTEMS NUSSLOCH...
The Issue: There is an issue regarding poorly processed and/or damaged biopsy tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama 1.0T HFO Recalled by Philips North America Llc Due to Firm was...
The Issue: Firm was informed of an event in which the structural integrity of the MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Valleylab FT10 Recalled by Covidien Due to Due to software issue,...
The Issue: Due to software issue, New systems may exhibit an error which may prohibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbsorbaTack Absorbable Fixation Device 30 Violet Absorbable Tacks 5 mm-...
The Issue: Packaging of the device may cause a low seal strength in the side seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty...
The Issue: Bandage Scissors handle cover component contains an incorrect color...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL...
The Issue: An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set Recalled by...
The Issue: There is to an increase in complaints related to failure alarms for Wet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE kits and trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoClean 3 Recalled by SoClean, Inc Due to New User Manual with additional...
The Issue: New User Manual with additional instructions for use and a hose and mask...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.