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. 1,989 recalls have been distributed to North Dakota in the last 12 months.
Showing 6441–6460 of 47,938 recalls
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 7 9 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyPoint Needle Recalled by Retractable Technologies, Inc. Due to The...
The Issue: The needle cannula of a retractable needle may detach from the needle holder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Aveir Leadless Pacemaker Recalled by Abbott Medical Due to Their is a...
The Issue: Their is a potential that electromagnetic interference may cause leadless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mesalamine Extended-Release Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neptune's Fix Recalled by Super Chill Products Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1 Recalled by...
The Issue: Subpotent Drug: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with Recalled by...
The Issue: Pack and pouch label is missing the manufacturing and expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing cabinets, running affected software, and Windows 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wash station: M1000 Wash Station Assembly & DITI Slide Recalled by Abbott...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.