Dr. Reddy's recalls 10 mg/mL Phytonadione Injectable Emulsion due to stability issues at 12-month testing. This may affect medication safety. Check NDC 43598-405-16 and lot numbers for affected products.
Failed Stability Specifications: Out of specification results reported at 12-month stability testing for aluminum content.
Dr. Reddy's is recalling a vitamin K injection product because stability tests showed aluminum content was out of specification after 12 months. This could mean the medication might not be safe for use after the expiration date.
The product failed stability testing at 12 months, showing aluminum content was outside acceptable limits. This could potentially affect the medication's safety and effectiveness over time.
Prescription patients using the recalled vitamin K injection. Healthcare providers who dispense this medication are most at risk.
Check for NDC code 43598-405-16 and lot number ACB101 on the product packaging. The product is a prescription-only vitamin K injection sold in 25 single-dose vials per carton.
Look for NDC 43598-405-16 and lot number ACB101 on the packaging.
The recall indicates stability issues were found in testing, but the product may still be safe for short-term use. Consult your healthcare provider for guidance.
Check for NDC code 43598-405-16 and lot number ACB101 on the packaging.
The recall does not specify a remedy, so contact your healthcare provider for advice on safe handling.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0007-2023 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0007-2023 from Dr. Reddy's. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.