Home / Recalls / Avella Of Deer Valley, Inc. Store 38 / D-0935-2018

D-0935-2018 Class II Terminated

Recalled by Avella Of Deer Valley, Inc. Store 38 — Phoenix, AZ

FDA drug recall D-0935-2018 was initiated by Avella Of Deer Valley, Inc. Store 38 on Jun 12, 2018 and is designated Class II. Reason for recall: Lack of Assurance of Sterility: Potential leakage of bags. The recall status is terminated (terminated Jan 24, 2020). Affected quantity: 275 syringes.

Recall Details

Product Type: Drugs
Report Date: Jul 25, 2018
Initiation Date: Jun 12, 2018
Termination Date: Jan 24, 2020
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 275 syringes

Product Description

HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 50 mg, 0.9% Sodium Chloride (USP) QS 50 mL) Volume: 50mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX. NDC 42852-222-65

Reason for Recall

Lack of Assurance of Sterility: Potential leakage of bags.

Distribution Pattern

Nationwide in the USA

Code Information

Lot # 5/16/18 1207 22265S, BUD 8/14/2018.

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0935-2018
openFDA file date: Oct 23, 2026
Loaded by RegDataLab: Oct 25, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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