← FDA ENFORCEMENT
D-0554-2025Class II

AEQUITA PHARMACY

Recalling firm
AEQUITA PHARMACY
Product type
Drug
Status
Ongoing
Report date
2025-08-13
Distribution
MA
Firm state
WA
Product quantity
236 vials
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Risk Management & CAPA
Reason for recall

Lack of Processing Controls.

Product description

Tirzepatide + Niacinamide 2.2 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.

Code / lot info

All Lots within expiry

Other recalls SPEQ maps to Risk Management & CAPA
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See all Risk Management & CAPA recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.