Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Ongoing Initiated May 7, 2024 (2 years ago)

Drug Vial Label: Zilretta¿

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6 weeks at 25 degrees C.

Cause type: Stability / shelf life

The product degraded or failed stability testing before its labeled expiry. Heat, moisture or time can break the drug down into degradants or reduce potency. All stability / shelf life recalls.

What was recalled

Drug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, Manufactured for: Pacira Pharmaceuticals Inc., San Diego, CA 92121, NDC 65250-001-01. Diluent Vial Label: Diluent, 5mL, Sterile single use, Rx only, Manufactured for Pacira Pharmaceuticals Inc., NDC 65250-002-01. Carton Label: Drug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, Manufactured for: Pacira Pharmaceuticals Inc., San Diego, CA 92121, NDC 65250-003-01.

Affected NDCs 65250-0001-01 65250-0002-01 65250-0003-01

Compare with the code on your package — it is the most precise check available.

Drug: Triamcinolone

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Zilretta
triamcinolone acetonide extended-release injectable suspension
NDC 65250-0003
Kit
Intra-Articular
Pacira Pharmaceuticals, Inc. Rx
Recalling firm
Pacira Pharmaceuticals INC
NDC code
65250-001-01
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0546-2024 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Triamcinolone recalls

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Class II · Moderate risk

Testosterone 100mg

Presence of Foreign substance - potential presence of metal particulate matter

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Other recalls by Pacira Pharmaceuticals INC

All 2024 recalls
Class II · Moderate risk

Exparel

Sub Potent Drug: Out of Specification (OOS)

Terminated Wrong potency / content Pacira Pharmaceuticals, Inc. D-0621-2020