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Class II: temporary or reversible health riskOngoing

Mckesson Medical-Surgical Inc. Corporate Office Medroxyprogesterone Acetate Injectable Recall

Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose V…

Mckesson Medical-Surgical Inc. Corporate Office · Richmond, VA

Risk level
Class II
Reported by FDA
May 7, 2025
Recall ID
D-0400-2025
Check your lot numberHow we source this data

Summary

Mckesson Medical-Surgical Inc. Corporate Office recalled Medroxyprogesterone Acetate Injectable starting Apr 25, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0400-2025 on May 7, 2025. Reason: Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product. Status: Ongoing.

Why it was recalled

Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.

Product description

Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-0330-01

Lot numbers, UPCs & expiration codes

Lot #: 1MP24042, Exp 6/30/26

Where it was sold

Distributed to Medical Facilities in MS and FL.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0400-2025
Classification
Class II
Status
Ongoing
Recall initiated
Apr 25, 2025
FDA report date
May 7, 2025
Quantity
3
Recall type
Voluntary: Firm initiated
Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office

Original FDA data

Every field from FDA enforcement report D-0400-2025, exactly as published.

Show all FDA fields
City
Richmond
State
VA
Status
Ongoing
Country
United States
Event ID
96744
Address
9954 Maryland Drive
Address (line 2)
Deep Run Iii Ste. 4000
Code information
Lot #: 1MP24042, Exp 6/30/26
Postal code
23233
Report date
May 7, 2025
Product type
Drugs
Recall number
D-0400-2025
Classification
Class II
Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
Product quantity
3
Reason for recall
Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-0330-01
Distribution pattern
Distributed to Medical Facilities in MS and FL.
Recall initiation date
Apr 25, 2025
Center classification date
May 1, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0400-2025, published May 7, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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