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. 1,785 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,785 in last 12 months

Showing 2974129760 of 47,938 recalls

Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Verathon Inc

Recalled Item: It is recommended for patients with weight/size between 4-22 lbs Recalled by...

The Issue: Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Merit Medical Systems, Inc.

Recalled Item: The PreludeSYNC Radial Compression Device is a sterile Recalled by Merit...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire with Flex Tip Recalled by...

The Issue: Cardiovascular Systems, Inc. is recalling one lot of ViperWire Advance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm) Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing