SKYN Non-Latex Condoms Recalled Due to Improper Storage
Family Dollar is recalling SKYN Original, Elite, and LS non-latex condoms due to improper storage. Products sold between May 1 and June 10, 2022 were not stored in temperature-controlled conditions.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall of a risk-of-harm medical device (contraception and STI prevention). Although no illnesses or injuries have been reported, improper storage of condoms could compromise material integrity and barrier effectiveness, posing a potential adverse health risk.
Plain-English summary
Family Dollar Stores, LLC is recalling SKYN Original Non-Latex Condoms (12-count, SKU 903409), SKYN Elite Non-Latex Condoms (12-count, SKU 903415), and SKYN LS Non-Latex Lubricated Condoms (3-count, SKU 900794). A total of 2,877 units were affected. The products were distributed to Family Dollar retail stores nationwide and sold between May 1, 2022 and June 10, 2022.
The products were not appropriately stored in temperature-controlled areas between April 30, 2022 and June 10, 2022. This storage deficiency prompted the recall.
Consumers who purchased these products are advised to contact Family Dollar Stores for information regarding the recall.
The recalled product
- Product
- SKYN ORIGINAL NON LATEX CONDOM 12CT, SKU 903409 LS SKYN NON LATEX LUBRICATED CONDOM 3CT, SKU 900794 SKYN ELITE NON LATEX CONDOM 12CT, SKU 903415
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Medical Device
- Affected units
- 2,877
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- All product sold between May 1
- 2022 - June 10
- 2022.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 22 recalled by Family Dollar Stores, Llc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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