Hydromorphone HCl 1 mg/mL 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.
Summary
The FDA issued a Class II for Hydromorphone HCl 1 mg/mL 250 mL bags, Rx only, Family Pharmacy of Statesville, by Family Pharmacy of Statesville. Reason: Lack of Assurance of Sterility.
Details
Source
Drug Recall
External ID
D-0657-2022
Action Date
2022-03-23
Status
Terminated
Category
drug
Product Description
Hydromorphone HCl 1 mg/mL 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.
Lot/Code Info: Lot #: 07272020@2 BUD: 10/25/2020; 07302020@1 BUD: 10/28/2020; 08012020@1 BUD: 10/30/2020
Quantity Affected: 4 bags
Reason for Recall
Lack of Assurance of Sterility
Distribution
NC only
Type: Voluntary: Firm initiated
Recall Initiated: 2020-08-06
Company
Statesville, NC
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 25 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Family Pharmacy of Statesville has 12 FDA actions in our database, including 12 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Family Pharmacy of Statesville) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Family Pharmacy of Statesville have FDA actions?
Family Pharmacy of Statesville has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0657-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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