Z-0822-2022Class II

Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana...

Name: Z-0822-2022 Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana...
Creator: Dollar Tree Distribution, Inc.
Published: 2022-02-18
License: https://open.fda.gov/license/

Dollar Tree Distribution, Inc. / initiated 2022-02-18 / Open, Classified

FDA source

Dollar Tree Distribution, Inc. began a recall of Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee. The general... on 2022-02-18. FDA classified it as Class II and gives the reason as "Potential exposure to rodents and rodent activity in the distribution center". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-0822-2022
Classification: Class II
Status: Open, Classified
Initiated: 2022-02-18
Posted: 2022-03-23
Recalling firm: Dollar Tree Distribution, Inc.
Product: 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
Product code: PWC General Wellness Product
Reason for recall: Potential exposure to rodents and rodent activity in the distribution center.
FDA root cause: Other
Action: On February 18, 2022, the recalling firm issued a press release notifying consumers of the recall. Additionally, the affected retail Family Dollar stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee were closed at 5 pm on February 18, 2022 for cleaning and to facilitate recalled product removal.
Quantity in commerce: Unknown
Distribution: US Nationwide distribution: Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee O.U.S.: N/A
Product codes and lots: 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.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0822-2022
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0822-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-03-30	2022-03-23

Product code PWC

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)