FDAClass II · Drug · Recall D-0811-2026 · Recalled September 9, 2026
Vasopressin recall — Baxter Healthcare Corporation
Agency report date: September 9, 2026.
1. Compare your item
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Agency product description and boundaries
Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL Single-Dose Container, Rx only, Sterile, Baxter Healthcare Corporation, Deerfield, IL, 60012 USA, NDC 0338-9640-12.
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If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
2. Agency hazard and consumer action
FDA reports: CGMP Deviations
No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.
Class II: may cause temporary or medically reversible health consequences.
Affected product: Vasopressin recall status
3. Open the official notice or contact
View the official FDA enforcement record (openFDA) ↗
Affected products
Companies & origin
Identifying details (verbatim from the notice)
Related recalls
More Baxter Healthcare recalls
- Dextrose Injection recall — Baxter Healthcare CorporationFDA · September 16, 2026
- 0 recall — Baxter Healthcare CorporationFDA · September 9, 2026
- Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall — Baxter Healthcare CorporationFDA · August 19, 2026
- Cefazolin in Dextrose recall — Baxter Healthcare CorporationFDA · August 19, 2026
- Hillrom VOLARA System P recall — Baxter Healthcare CorporationFDA · July 8, 2026
Other drug recalls from around the same time
- 0 recall — B BRAUN MEDICAL INCFDA · September 16, 2026
- Epinephrine Injection recall — American Regent, Inc.FDA · September 16, 2026
- Glutathione 200 mg/mL recall — OPTIMAL BALANCE PHARMACYFDA · September 9, 2026
- Lactated Ringer's Injection USP recall — B BRAUN MEDICAL INCFDA · September 2, 2026
- Tyenne (tocilizumab-aazg) Injection recall — Fresenius Kabi USA, LLCFDA · September 2, 2026
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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.