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. 2,668 recalls have been distributed to Delaware in the last 12 months.
Showing 5321–5340 of 27,373 recalls
Recalled Item: NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal...
The Issue: May have increased water path restriction within the heat exchanger, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal...
The Issue: May have increased water path restriction within the heat exchanger, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RANDOX Total Bilirubin. Recalled by Randox Laboratories Ltd. Due to Randox...
The Issue: Randox has had reports of elevated patient results using Plasma (lithium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline manual resuscitators with integrated manometer Recalled by SunMed...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD gravity sets (Product Name Recalled by Becton Dickinson & Company Due to...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Extension Sets (Product Name Recalled by Becton Dickinson & Company Due...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex manual resuscitators with integrated manometer Recalled by SunMed...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump infusion sets (Product Name Recalled by Becton Dickinson &...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System Product Code 6844458 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Product Code 6802445 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.