FDA Recall of Vancomycin HCI Injection by Fagron Compounding Services
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Fagron Compounding Services is voluntarily recalling 34,260 bags of Vancomycin HCI injection due to concerns over lack of sterility and potential detachment of a part.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 22, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Drugs.
Recall Article
What Happened
Fagron Compounding Services is recalling the product due to a lack of assurance of sterility and the possibility that the blue Break-Off-Part could detach from the administration port.
Which Products Are Affected
The affected product is Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, with NDC 71266-5083-01. A total of 34,260 bags are involved, distributed nationwide in the U.S.A. The specific lots and expiration dates are: C274-000050857 (Exp. 7/6/2026), C274-000049316 (Exp. 4/26/2026), C274-000049367 (Exp. 4/28/2026), C274-000049496 (Exp. 5/3/2026), C274-000049518 (Exp. 5/4/2026), C274-000049535 (Exp. 5/5/2026), C274-000049653 (Exp. 5/11/2026), C274-000049654 (Exp. 5/11/2026), C274-000049745 (Exp. 5/16/2026), C274-000050128 (Exp. 5/31/2026), C274-000050151 (Exp. 6/1/2026), C274-000050184 (Exp. 6/6/2026), C274-000050504 (Exp. 6/15/2026), C274-000050662 (Exp. 6/21/2026), C274-000050836 (Exp. 7/5/2026), C274-000051014 (Exp. 7/13/2026), C274-000051057 (Exp. 7/18/2026), and C274-000051240 (Exp. 7/25/2026). The recall number is D-0440-2026.
What You Should Do
Consumers should follow the initial firm notification, which was sent via letter, for instructions. For returns or refunds, contact Fagron Compounding Services at 8710 E 34th St N, Wichita, KS 67226-2636.
Why This Matters
This recall affects a significant quantity of a drug product, potentially impacting patient safety due to sterility issues in nationwide distribution.
Source
FDA Recall Number: D-0440-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
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Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,564 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 22, 2026.
Frequently Asked Questions
Common questions about this FDA recall.