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. 1,012 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,012 in last 12 months

Showing 17321–17340 of 47,938 recalls

DrugAugust 14, 2020· Grupo Asimex de Mexico SA de CV

Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...

The Issue: CGMP Deviations: All other lots are being recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 14, 2020· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...

The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Battelle Memorial Institute

Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...

The Issue: Masks processed at one site were not maintained at levels of condensation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Sobel Westex

Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...

The Issue: Due to non-surgical isolation gowns not meeting all performance test...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Pharmaceutical Innovations, Inc.

Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...

The Issue: The firm registered the product as a Class I device, but has since been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...

The Issue: Connector between support surface and pump may be out of tolerance resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrogenase L-P Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market El Trigal 12 Month Old Manchego PLU 29329500000 Recalled...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market Mitica Mahon PLU 29341800000 Individual sliced cheese...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund