Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Epi-Caine Recalled by Pine Pharmaceuticals, LLC Due to CGMP Deviations: Raw material recalled by repackager, due...

Date: December 22, 2022
Company: Pine Pharmaceuticals, LLC
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Pine Pharmaceuticals, LLC directly.

Affected Products

Epi-Caine, Epinephrine 0.025% Lidocaine HCL 0.75% Solution for Intraocular Injection, 1 ml, Single Dose Vial, Compounded by Pine Pharmaceuticals, 355 Riverwalk Pkwy, Tonawanda, NY 14150. NDC 69194-0948-1

Quantity: 11,453 vials

Why Was This Recalled?

CGMP Deviations: Raw material recalled by repackager, due to discoloration.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Pine Pharmaceuticals, LLC

Pine Pharmaceuticals, LLC has 24 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report