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Potassium Acetate Injection, USP 40 mEq/20 mL (2 mEq/mL) Single Dose Vials, Rx only, Manufacture...

FDA Recall #D-1585-2020 — Class III — May 5, 2020

Recall #D-1585-2020 Date: May 5, 2020 Classification: Class III Status: Terminated

Product Description

Potassium Acetate Injection, USP 40 mEq/20 mL (2 mEq/mL) Single Dose Vials, Rx only, Manufactured By: Exela Pharma Sciences, LLC. Lenoir, NC NDC 51754-2001-4

Reason for Recall

Short Fill

Recalling Firm

Exela Pharma Sciences LLC — Lenoir, NC

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

23,775 vials

Distribution

Nationwide and Puerto Rico

Code Information

Lot #P0000471, Catalog #2020TS002, Exp Date: 04/2021

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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