Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,478 recalls have been distributed to Minnesota in the last 12 months.
Showing 28481–28500 of 52,120 recalls
Recalled Item: Trimix #23F (Prostaglandin E1 6 mcg/ Papaverine HCl 17.8 mg/ Recalled by KRS...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin 500 mcg Orally Disintegrating Tablets (ODT) Recalled by KRS...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benzocaine 20% Recalled by KRS Global Biotechnology, Inc Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T-105 (Prostaglandin E1 Recalled by KRS Global Biotechnology, Inc Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chloramphenicol 500 mg Amphotericin 50 mg Otic Powder packaged in jars...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule Recalled by KRS...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Anastrozole SR 1 mg Capsules Recalled by KRS Global Biotechnology, Inc Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxocobalamin 1 mg/mL 30 mL Vial For IM Use Recalled by KRS Global...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin Acetate 3 mg/ GHRP6 3 mg Recalled by KRS Global Biotechnology,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated...
The Issue: Potential for cracked luer hubs
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) Spectra...
The Issue: The Spectra System/Legacy Guided Surgery Handle Kit had guided handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen CVC Kit Recalled by Arrow International Inc...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath Recalled by...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.