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. 2,540 recalls have been distributed to North Dakota in the last 12 months.
Showing 6761–6780 of 47,938 recalls
Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...
The Issue: X-ray exposure termination audible signal on Senographe Pristina with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...
The Issue: Knee batteries may need replacement with conforming batteries to ensure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to a case Recalled...
The Issue: Undeclared Yellow #5
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Americaine Recalled by Insight Pharmaceuticals LLC, a Prestige Consumer...
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bleomycin for Injection Recalled by PFIZER Due to Presence of particulate...
The Issue: Presence of particulate matter: glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Good Neighbor Pharmacy Recalled by Pharma Nobis LLC Due to MICROBIAL...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence of...
The Issue: Presence of Particulate Matter; identified as glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4 % Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence...
The Issue: Presence of Particulate Matter; identified as glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atropine Sulfate Injection Recalled by Pfizer Inc. Due to Presence of...
The Issue: Presence of Particulate Matter; identified as glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Walgreens Dye-Free Magnesium Citrate Saline Laxative/Oral Solution Recalled...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG Recalled by AMD Medicom Inc....
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)...
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item...
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.