Class III โ€” Low Risk

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

Xanax (Alprazolam) USP Recalled by Mckesson Packaging Services Due to Labeling: Missing Label-Primary packaging label (i.e. blister card)...

Date: September 15, 2016
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

Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC 63739-669-10

Quantity: 3,492 unit cartons of 10 x 10 blister cards

Why Was This Recalled?

Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).

Where Was This Sold?

This product was distributed to 4 states: CO, IL, LA, OH

Affected (4 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