Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Aspirin DR Enteric Coated Tablets Recalled by Mckesson Packaging Services Due to Failed Dissolution Specification; at the 12 month time...

Date: June 19, 2014
Company: Mckesson Packaging Services
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 Mckesson Packaging Services directly.

Affected Products

Aspirin DR Enteric Coated Tablets, USP 325 mg, UD 750 tablets (25x30), Dist. By: McKesson Packaging Services a business unit of McKesson Corporation, concord, NC

Quantity: 1,511,250 tablets

Why Was This Recalled?

Failed Dissolution Specification; at the 12 month time interval.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Mckesson Packaging Services

Mckesson Packaging Services has 14 total recalls tracked by RecallDetector.

Related Recalls

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