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. 1,032 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,032 in last 12 months

Showing 15561–15580 of 47,938 recalls

FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE NEOPOLITAN ICE CREAM DIETARY SUPPLEMENT...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: HI-TECH PHARMACEUTICALS PRECISION PROTEIN COOKIES & CREAM NET WT 2lbs...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE VANILLA MILKSHAKE DIETARY SUPPLEMENT NET WT....

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE VANILLA ICE CREAM DIETARY SUPPLEMENT NET WT....

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY SUPPLEMENT...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: IFN iFORCE NUTRITION MASS GAINZ PROTEIN MATRIX BROWN SUGAR MAPLE Recalled by...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE MILKSHAKE DIETARY SUPPLEMENT NET...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE FUDGE POP DIETARY SUPPLEMENT...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE ORANGE CREAMSICLE DIETARY SUPPLEMENT NET WT....

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 2, 2021· Starwest Botanicals, Inc

Recalled Item: Starwest Botanicals Item#: 209617-34 Recalled by Starwest Botanicals, Inc...

The Issue: Presence of E. coli species

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2021· Merits Holdings Co. dba Merits Health Products, Inc.

Recalled Item: Power Wheelchair Recalled by Merits Holdings Co. dba Merits Health Products,...

The Issue: Seat baseplate pin has broken in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· CLINICAL LASERTHERMIA SYSTEMS AB

Recalled Item: Tranberg MR Stylet Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...

The Issue: single use devices labeled as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· CLINICAL LASERTHERMIA SYSTEMS AB

Recalled Item: Tranberg MR Cannula Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...

The Issue: single use devices labeled as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· CLINICAL LASERTHERMIA SYSTEMS AB

Recalled Item: Tranberg Laser Applicator Non-cooled Recalled by CLINICAL LASERTHERMIA...

The Issue: single use devices labeled as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· Merits Holdings Co. dba Merits Health Products, Inc.

Recalled Item: Scooter Recalled by Merits Holdings Co. dba Merits Health Products, Inc. Due...

The Issue: Seat baseplate pin has broken in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· Stryker Leibinger GmbH & Co. KG

Recalled Item: DirectInject consists of a sterile dual paste system which is Recalled by...

The Issue: Inability for the user to inject the paste from the syringe into the target...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: ACE MDI Spacer with Small Mask - Product Usage: designed Recalled by Smiths...

The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Palm Cups - Product Usage: intended to be used to Recalled by Smiths Medical...

The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...

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

Class II — Potential Health HazardOngoing