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U.S. Department of Health and Human Services

Class 2 Device Recall General wellness products

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 Class 2 Device Recall General wellness productssee related information
Date Initiated by FirmFebruary 18, 2022
Create DateMarch 23, 2022
Recall Status1 Open3, Classified
Recall NumberZ-0822-2022
Recall Event ID 89658
Product Classification General wellness product - Product Code PWC
ProductMedical 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
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.
FEI Number 1000123383
Recalling Firm/
Manufacturer		 Dollar Tree Distribution, Inc.
500 Volvo Pkwy
Chesapeake VA 23320-1604
For Additional Information Contact Kayleigh Campbell
757-321-5001
Manufacturer Reason
for Recall		Potential exposure to rodents and rodent activity in the distribution center.
FDA Determined
Cause 2		Other
ActionOn 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 CommerceUnknown
DistributionUS Nationwide distribution: Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee O.U.S.: N/A
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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