Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi,
Summary
The FDA issued a Class II for Medical Device products purchased from Family Dollar retail stores located in Al by Dollar Tree Distribution, Inc.. Reason: Potential exposure to rodents and rodent activity in the distribution center..
Details
Source
Device Recall
External ID
Z-0822-2022
Action Date
2022-03-30
Status
Ongoing
Category
device
Product Description
Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee. The general categories of products, but are limited to these products, includes: feminine hygiene products, surgical masks, contact lens cleaning solutions, bandages, nasal care products
Lot/Code Info: All medical device products purchased from Family Dollar retail stores located in AL, AR, LA, MS, MO, and TN from January 1, 2021 to present.
Quantity Affected: Unknown
Reason for Recall
Potential exposure to rodents and rodent activity in the distribution center.
Distribution
US Nationwide distribution: Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee O.U.S.: N/A
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-18
Company
Chesapeake, VA
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 146 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Dollar Tree Distribution, Inc. has 5 FDA actions in our database, including 5 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 (Dollar Tree Distribution, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dollar Tree Distribution, Inc. have FDA actions?
Dollar Tree Distribution, Inc. has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0822-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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