Severity
Moderate
ModerateClass IIOngoing
FDA Drug recall · Reported August 6, 2025
Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04
CGMP Deviations; particulates identified during visual inspection
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Pfizer Inc. recalled Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4… - a moderate-severity action.
Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4… was recalled by Pfizer Inc. in August 6, 2025. Reason: CGMP Deviations; particulates identified during visual inspection. Check the official notice for the remedy. Verify recall #D-0545-2025 with the FDA Drug before acting.
The recall
Pfizer Inc. issued this moderate-severity FDA Drug recall-CGMP Deviations; particulates identified during visual inspection.
- Moderate
- severity level
- Class II
- classification
- August 6, 2025
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0545-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0545-2025) was formally reported on August 6, 2025, with the manufacturer initiating the action on July 10, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Pfizer Inc. is listed as the recalling firm, operating out of New York, NY. Federal records list the affected scope as 19,279 vials.
The documented reason for this recall is: CGMP Deviations; particulates identified during visual inspection Distribution data in the federal record shows the product reached: Nationwide in the USA. 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 - 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.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices 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
19,279 vials
Related Recalls
6
0 from same agency
Product description
Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04
Reason for recall
CGMP Deviations; particulates identified during visual inspection
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0545-2025 |
| Date reported | August 6, 2025 |
| Date initiated | July 10, 2025 |
| Recalling firm | Pfizer Inc. |
| Firm location | New York, NY |
| Affected scope | 19,279 vials |
| Distribution | Nationwide in the USA |
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-0545-2025) 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? ▼
Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04. Recalled by Pfizer Inc.. Units affected: 19,279 vials.
Why was this product recalled? ▼
CGMP Deviations; particulates identified during visual inspection
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 6, 2025. Severity: Moderate. Recall number: D-0545-2025.
Where was the recalled product distributed? ▼
Distribution: Nationwide in the USA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0545-2025) 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
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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 August 6, 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.