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. 2,363 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,363 in last 12 months

Showing 2708127100 of 27,512 recalls

Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit Recalled by ICU...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2012· Berchtold Corp.

Recalled Item: OPERON D850 Surgical Table Product Usage: Surgical Table Recalled by...

The Issue: Table was not lowering.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2012· Maquet Medical Systems, Usa

Recalled Item: Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table Top...

The Issue: As a result of a small number of customer complaints, MAQUET conducted an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Becton Dickinson & Co.

Recalled Item: BD Gram Stain Kit Recalled by Becton Dickinson & Co. Due to Potential for...

The Issue: Potential for increase level of artifacts to appear as large, spherical and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Becton Dickinson & Co.

Recalled Item: Gram Crystal Violet 250 mL Recalled by Becton Dickinson & Co. Due to...

The Issue: Potential for increase level of artifacts to appear as large, spherical and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Varian Medical Systems, Inc.

Recalled Item: Rectal Retractors Recalled by Varian Medical Systems, Inc. Due to A medical...

The Issue: A medical device used in brachytherapy may become contaminated and can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Varian Medical Systems, Inc.

Recalled Item: Rectal Retractors Recalled by Varian Medical Systems, Inc. Due to A medical...

The Issue: A medical device used in brachytherapy may become contaminated and can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Beckman Coulter Inc.

Recalled Item: AutoMate 1250 and AutoMate 2550 Recalled by Beckman Coulter Inc. Due to The...

The Issue: The recall was initiated because Beckman Coulter has confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E is a multi-purpose SPECT system used to detect Recalled by Siemens...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: E.CAM emission computed tomography system used to detect or image Recalled...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· Kerr Corporation

Recalled Item: The brand name of the device is Laser Loupes Recalled by Kerr Corporation...

The Issue: The firm initiated the recall for Laser Loupes because the ink used to mark...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2012· Gulf Fiberoptics, Inc.

Recalled Item: GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink. GMF-RC65...

The Issue: The GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink falls...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC...

The Issue: ConMed Linvatec is recalling the product due to the punch being...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Invacare Corporation

Recalled Item: TDX SP Power Wheelchair Recalled by Invacare Corporation Due to Invacare...

The Issue: Invacare Corporation decided to recall the product because of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Steris Corporation

Recalled Item: STERIS 5085 and 5085 SRT Surgical Tables Recalled by Steris Corporation Due...

The Issue: STERIS has learned from Customer feedback and field service experience that...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Etac Supply Center Ab

Recalled Item: Etac¿ Ono Walker Recalled by Etac Supply Center Ab Due to The recall has...

The Issue: The recall has been initiated because there is the potential that users may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima Mobile X-ray System. The GE Automatic Mobile Recalled...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2012· Ethicon, Inc.

Recalled Item: Ethicon Surgiflo Hemostatic Matrix Kit with Thrombin Plus Flex Tip Recalled...

The Issue: The lyophilized thrombin component of the Surgiflo Hemostatic Matrix kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2012· Beckman Coulter Inc.

Recalled Item: Unicel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the UniCel DxH 800 Coulter Cellular Analysis...

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

Class II — Potential Health HazardOngoing