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Hydromorphone (0.2 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Housto...

FDA Recall #D-0133-2019 — Class II — October 19, 2018

Recall #D-0133-2019 Date: October 19, 2018 Classification: Class II Status: Terminated

Product Description

Hydromorphone (0.2 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38

Reason for Recall

Lack of assurance of sterility

Recalling Firm

Avella of Deer Valley, Inc. Store 38 — Phoenix, AZ

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

360 bags

Distribution

U.S.A. nationwide.

Code Information

Lot # 8/27/18 0215 22110P, Exp 12/10/2018

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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