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. 1,017 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,017 in last 12 months

Showing 16401–16420 of 48,330 recalls

Medical DeviceJanuary 19, 2021· Boston Scientific Corporation

Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...

The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· ReNovo, Inc.

Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...

The Issue: Non-sterile product was shipped to customers labelled as sterile.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Boston Scientific Corporation

Recalled Item: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares...

The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Sky Medical Supplies and Equipments LLC

Recalled Item: AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM...

The Issue: Distributed COVID test kits without emergency use authorization.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Boston Scientific Corporation

Recalled Item: Captivator Single-Use Polypectomy Snares Recalled by Boston Scientific...

The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2021· Smiths Medical ASD Inc.

Recalled Item: Tube Tracheostomy and Tube Cuff Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Smiths Medical became aware that three lot numbers of a specific model of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Northgate Technologies, Inc.

Recalled Item: Steris CO2MPACT Endoscopic Insufflator system Recalled by Northgate...

The Issue: An internal tubing component in the flow path was made with incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Northgate Technologies, Inc.

Recalled Item: ConMed 50L abdominal insufflator Recalled by Northgate Technologies, Inc....

The Issue: An internal tubing component in the flow path was made with incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Biomet, Inc.

Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Hamilton Co

Recalled Item: HAMILTON HEATER SHAKER Recalled by Hamilton Co Due to There is a risk that...

The Issue: There is a risk that the device can start a fire if flammable liquids...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing