Severity
Moderate
ModerateClass IIOngoing
FDA Drug recall · Reported May 7, 2025
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
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…
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Mckesson Medical-Surgical Inc. Corporate Office recalled Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Via… - a moderate-severity action.
Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Via… was recalled by Mckesson Medical-Surgical Inc. Corporate Office in May 7, 2025. Reason: Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 an…. Check the official notice for the remedy. Verify recall #D-0400-2025 with the FDA Drug before acting.
The recall
Mckesson Medical-Surgical Inc. Corporate Office issued this moderate-severity FDA Drug recall-Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 an….
- Moderate
- severity level
- 3 units
- affected scope
- Class II
- classification
- May 7, 2025
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0400-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0400-2025) was formally reported on May 7, 2025, with the manufacturer initiating the action on April 25, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Mckesson Medical-Surgical Inc. Corporate Office is listed as the recalling firm, operating out of Richmond, VA. Federal records list the affected scope as 3.
The documented reason for this recall is: 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 product… Distribution data in the federal record shows the product reached: Distributed to Medical Facilities in MS and FL.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
3
Related Recalls
6
5 from same agency
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
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0400-2025 |
| Date reported | May 7, 2025 |
| Date initiated | April 25, 2025 |
| Recalling firm | Mckesson Medical-Surgical Inc. Corporate Office |
| Firm location | Richmond, VA |
| Affected scope | 3 |
| Distribution | Distributed to Medical Facilities in MS and FL. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0400-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Mckesson Medical-Surgical Inc. Corporate Office. Units affected: 3.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 7, 2025. Severity: Moderate. Recall number: D-0400-2025.
Where was the recalled product distributed? ▼
Distribution: Distributed to Medical Facilities in MS and FL..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0400-2025) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3…
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported May 7, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.