← Search recalls
FDA (Device enforcement)Recalled 2013-01-14closedclass ii

Ansell Healthcare Products LLC: LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell Healthcare Products LLC, Dothan, AL 96303. A sheath which completely covers the penis with a clos

Is my product affected?

LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell Healthcare Products LLC, Dothan, AL 96303. A sheath which completely covers the penis with a closely fitting membrane. The condom is used for contraceptive and for prophylactic purposes (preventing transmission of sexually transm

  • UPC 30070907205106

Check against the official notice below — it lists the full affected range.

What happened

Ansell Healthcare Products LLC is recalling LifeStyles ZERO 10 uber-thin lubricated latex condoms manufactured for distribution nationwide. The company received complaints about difficulty unrolling the condoms and subsequent breakage, prompting the voluntary recall as a precaution, even though the product met or exceeded FDA test and quality standards. Approximately 469,134 units with SKU# 0-70907-20510-5 and Master Case code 30070907205106 are affected across multiple states including Alabama, Arizona, California, Colorado, Delaware, Florida, Georgia, Iowa, Indiana, Illinois, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Hampshire, New Jersey, New York, Ohio, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Wisconsin, and Utah.

The recall source does not specify a remedy or instructions for consumers to follow.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Out of an abundance of caution, Ansell is implementing a voluntary recall of the Zero Latex Condom (regular) product. The condom has met or exceeded test and quality standards required by the Food and Drug Administration. However, we are experiencing a number of complaints concerning the difficulty in unrolling and subsequent breakage, and so we are asking to have all products returned.

Details from the source

Reason for recall: Out of an abundance of caution, Ansell is implementing a voluntary recall of the Zero Latex Condom (regular) product. The condom has met or exceeded test and quality standards required by the Food and Drug Administration. However, we are experiencing a number of complaints concerning the difficulty in unrolling and subsequent breakage, and so we are asking to have all products returned. Distribution: .Nationwide Distribution including the states of AL, AZ, CA, CO, DE, FL, GA, IA, IN, IL, KS, KY, LA, MI, MN, MO.MS, NC, NH, NJ, NY, OH, OR, PA, RI, SC, TN, TX, VA, WI and UT. Quantity: 469,134 units Lot/code info: Zero Regular 10-Ct: SKU# 0-70907-20510-5 Master Case: 30070907205106.

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

Related recalls

All FDA (Device enforcement) recalls

Hurt by this product? Start a free Case Check

ProductRisk is not a law firm and does not provide legal services or legal advice. ProductRisk is a free consumer product-safety information service operated by Plaintify, Inc., a technology company. If you ask to be connected with a law firm, any legal services are provided by that firm — not by ProductRisk or Plaintify.

Privacy · Plaintify