← FDA ENFORCEMENT
D-0374-2024Class II

Thea Pharma, Inc.

Recalling firm
Thea Pharma, Inc.
Product type
Drug
Status
Terminated
Report date
2024-03-20
Distribution
Product was distributed nationwide within the United States
Firm state
MA
Product quantity
5,476 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Lack of Assurance of Sterility: Out of specification for volume and compromised container closure.

Product description

Betimol (timolol ophthalmic solution) 0.5%, 15mL bottles, Rx only, Manufactured for: Thea Pharma Inc. Lexington, MA 02420, NDC 82584-002-15

Code / lot info

Lot #: 435019, Exp. Date 11/2024

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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.