Z-1546-2022Class II

Lifestyles Ultra Sensitive Condoms 12Ct, Sku 900265

Name: Z-1546-2022 Lifestyles Ultra Sensitive Condoms 12Ct, Sku 900265
Creator: Family Dollar Stores, Llc.
Published: 2022-06-23
License: https://open.fda.gov/license/

Family Dollar Stores / initiated 2022-06-23 / Open, Classified

FDA source

Family Dollar Stores, Llc. began a recall of LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT, SKU 900265 on 2022-06-23. FDA classified it as Class II and gives the reason as "Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-1546-2022
Classification: Class II
Status: Open, Classified
Initiated: 2022-06-23
Posted: 2022-08-17
Recalling firm: Family Dollar Stores
Product: Lifestyles Ultra Sensitive Condoms 12Ct, Sku 900265
Product code: HIS Condom
Reason for recall: Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
FDA root cause: Storage
Action: On June 23, 2022, the firm notified affected Family Dollar retail stores via an urgent Pull and Hold notice, effective June 24, 2022. Retail stores were informed that due to a shipping issue, the affected products could not be sold. Stores were instructed to remove affected products from the sales floor and quarantine them. https://www.familydollar.com/file/general/Voluntary_Recall_of_Certain_Over_the_Counter_Products_080522.pdf
Quantity in commerce: 5
Distribution: Product distributed to Family Dollar retail stores in US nationwide.
Product codes and lots: All product sold between May 1, 2022 - June 10, 2022.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1546-2022
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1526-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1527-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1528-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1529-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1530-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1531-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1532-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1533-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1534-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1535-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1536-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1537-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1538-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1539-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1540-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1541-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1542-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1543-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1544-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1545-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1546-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17
Z-1547-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-08-24	2022-08-17

Product code HIS

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)