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. 2,531 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,531 in last 12 months

Showing 98619880 of 47,938 recalls

DrugJanuary 30, 2023· IBSA PHARMA INC

Recalled Item: TIROSINT - SOL (levothyroxine sodium) Oral Solution Recalled by IBSA PHARMA...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 30, 2023· Akorn, Inc.

Recalled Item: Atropine Sulfate Ophthalmic Solution Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Stability Specifications: Out of specification test results for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 30, 2023· Maquet Cardiovascular, LLC

Recalled Item: Fusion Bioline Vascular Graft Recalled by Maquet Cardiovascular, LLC Due to...

The Issue: One (1) Fusion Bioline Vascular graft from lot 25162546, which failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test...

The Issue: Siemens Healthineers has received customer complaints and confirmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa COVID-19 Direct Recalled by DiaSorin Molecular LLC Due to Direct...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Carefusion 2200 Inc

Recalled Item: CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog...

The Issue: Product did not meet shelf-life testing requirements resulting in a breach...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa Flu A/B & RSV Direct Gen II Recalled by DiaSorin Molecular LLC Due...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Carestream Health, Inc.

Recalled Item: DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For...

The Issue: After pressing and releasing the Z-Axis Motorized buttons on the Tube Head...

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

Class II — Potential Health HazardOngoing
FoodJanuary 28, 2023· Pepsico Inc

Recalled Item: Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 Fl Oz (405mL)....

The Issue: Foreign object (glass).

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2023· Amerisource Health Services LLC

Recalled Item: Verapamil Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides (concentrated)-In vitro diagnostic use in the...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH LDL Cholesterol Direct (DLDL)-In vitro diagnostic quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Total Protein II- In vitro diagnostic use in Recalled by Siemens...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides_2: in vitro diagnostic use in the quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· Beckman Coulter, Inc.

Recalled Item: Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N)...

The Issue: An increased incidence of damage to the nut band from a new vendor (Boamax)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· CooperVision, Inc.

Recalled Item: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)...

The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· CooperVision, Inc.

Recalled Item: Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens...

The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Church & Dwight Inc

Recalled Item: Easy Read App associated with First Response Pregnancy Test Sticks Recalled...

The Issue: Church & Dwight First Response Pregnancy Kits was marketed with the Easy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Covidien, LP

Recalled Item: Tri-Staple 2.0 Black Intelligent Reload Recalled by Covidien, LP Due to...

The Issue: Affected lots have the potential for a broken sled vane, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Stryker Corporation

Recalled Item: Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the...

The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...

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

Class II — Potential Health HazardOngoing