Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 992 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
992 in last 12 months

Showing 21161–21180 of 47,938 recalls

Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 19FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Medline Silicone Drain 15Fr 3/16" Full Fluted PN: DYNJWE2188HB An Recalled...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Sentinel CH SpA

Recalled Item: Alinity c Lithium Reagent Kit- intended for the quantitation of Recalled by...

The Issue: Added an additional SmartWash parameter for the Lithium and Alinity c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 15FR Cardinal PN:JP-2223 An...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 19FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Smith & Nephew Negative Pressure Wound Therapy 15FR Channel Wound Recalled...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2019· Fresenius Kabi USA, LLC

Recalled Item: Fluorouracil Injection Recalled by Fresenius Kabi USA, LLC Due to Presence...

The Issue: Presence of Particulate Matter; glass particulates

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
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· 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· Baxter Healthcare Corporation

Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...

The Issue: EXACTAMED 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 10 mL...

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

Class III — Low RiskOngoing
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· 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· 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