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. 2,572 recalls have been distributed to Delaware in the last 12 months.
Showing 17361–17380 of 27,373 recalls
Recalled Item: Large Stealth Chamber Recalled by Iba Dosimetry Due to When the Stealth...
The Issue: When the Stealth Chamber is used as a detector in relative dosimetry,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarke-Reich Laparoscopic Knot Pusher Recalled by Cook Inc. Due to...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ IV Premium Catheter Stabilization Device Recalled by Bard Access...
The Issue: StatLockTM IV Premium Catheter Stabilization Device may contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra Ligature Carrier 75 Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra-Raz Ligature Carrier Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST ETP32 (Ertapenem) Ref. 531640 Recalled by BioMerieux SA Due to False...
The Issue: False susceptible results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Introducer/Extractor Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venture RX Catheter Recalled by Vascular Solutions, Inc. Due to Vascular...
The Issue: Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microalbumin Reagent Recalled by Beckman Coulter Inc. Due to Beckman Coulter...
The Issue: Beckman Coulter has confirmed that MA Reagent Lot M609458 may recover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips V60 Ventilators Recalled by Respironics California Inc Due to Over...
The Issue: Over time, low-frequency vibrations can cause the pins within the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brennen Skin Graft Mesher. Surgical instrument designed to expand skin...
The Issue: Sterilization validation failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE CONNECTOR 3/8 Y 20/BX Recalled by Teleflex Medical Due to Labeling: The...
The Issue: Labeling: The expiration date is not stated on the labeling, there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain Recalled by...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.