Z-0822-2022 Class II Ongoing
FDA device recall Z-0822-2022 was initiated by Dollar Tree Distribution, Inc. on Feb 18, 2022 and is designated Class II. Reason for recall: Potential exposure to rodents and rodent activity in the distribution center. The recall status is ongoing.
Recall Details
- Product Type
- Devices
- Report Date
- Mar 30, 2022
- Initiation Date
- Feb 18, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
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
Reason for Recall
Potential exposure to rodents and rodent activity in the distribution center.
Distribution Pattern
US Nationwide distribution: Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee O.U.S.: N/A
Code Information
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.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0822-2022
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026