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. 997 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
997 in last 12 months

Showing 21401–21420 of 48,330 recalls

Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: MiniMed Paradigm Model 511 Insulin Pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: N Cuvette Segments for BN ProSpec System-IVD a system for Recalled by...

The Issue: Iincreased (falsely elevated) Albumin results compared to expected results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Veo Insulin pump Recalled by Medtronic MiniMed...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Agfa N.V.

Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Recalled by Agfa...

The Issue: The exposed area of fluo exams possibly does not match the active area of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: MiniMed Insulin Pump Recalled by Medtronic MiniMed Due to The action is...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x95 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 1.6x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x38 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x110 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 1.1x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing