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Serious recall: Injury is possible or has been reported. Take action promptly.

SUN PHARMACEUTICAL INDUSTRIES INC 2022-06-22 Health serious FDA
Health · FDA · Recall #FDA-D-1144-2022

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150… Recall

Issued June 22, 2022 · SUN PHARMACEUTICAL INDUSTRIES INC

In June 2022, SUN PHARMACEUTICAL INDUSTRIES INC recalled the medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Lack of assurance of sterility

What you should do

  1. 1 Stop using medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact SUN PHARMACEUTICAL INDUSTRIES INC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
SUN PHARMACEUTICAL INDUSTRIES INC
Category
Health
Recall date
June 22, 2022
Units affected
Not reported
Sold at
USA Nationwide
Recall number
FDA-D-1144-2022
Made in
United States
Issuing agency
FDA

In context

  • SUN PHARMACEUTICAL INDUSTRIES INC has 34 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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