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HEALTH ALERT – Around 7 million condoms recalled across Europe over risk of tearing and perforation

Manufacturing defects in several ranges of ultra-thin condoms have led the French authorities to order the withdrawal and recall of 15 product references sold in Europe. Consumers are being urged to stay vigilant given the risks of sexually transmitted infections and unwanted pregnancies.

The Radio Tripoint newsroom 2 min read Thionville
HEALTH ALERT – Around 7 million condoms recalled across Europe over risk of tearing and perforation

A Europe-wide health alert. On 30 October 2026, the French Ministry of the Economy announced the suspension of sales and imports of several references of ultra-thin condoms made by the Malaysian company Richter Rubber Technology.

The decision follows defects found during inspections and laboratory analyses. The investigations revealed irregularities in the thickness and quality of the latex film used in manufacturing. These anomalies can cause perforations or tears during use.

15 references affected, around 7 million products in Europe

According to the French authorities, the products concerned amount to around 7 million condoms distributed on the European market. Only some of these products were sold in France.

The brands and references affected include:

  • My Lubie Ultra Fin
  • Einhorn Condoms
  • Releaf
  • Vitalis Super Thin
  • Prevento Feelings
  • ON Super Thin
  • Naked Tested & Rolled
  • Primeros Innocent
  • You+Me Darling

This list is not exhaustive. References and batch numbers must be checked against the official recall notices.

Potential health consequences

The defects identified may compromise the effectiveness of these methods of contraception and protection.

Since the first recalls, eight users have reported condoms tearing that matched batches found by analysis to be non-compliant and dangerous.

The risks identified mainly concern:

  • The transmission of sexually transmitted infections (STIs).
  • Unwanted pregnancies.

The authorities advise anyone who has used the products concerned to get tested for STIs at a medical laboratory. If a period is late, a pregnancy test is also recommended.

What should you do if you have one of these products?

Consumers are advised to:

  • Stop using the condoms concerned.
  • Check the brand, reference and batch number.
  • Contact the retailer to find out how to return the product.
  • Seek advice from a healthcare professional or a testing centre (CeGIDD) if they have used an affected product.

Vigilance across borders

In a region such as the Three Borders area, where residents travel daily between France, Luxembourg and Germany, this information deserves particular attention.

Online shopping and cross-border distribution channels make it essential to check the references and batches concerned.

The case is also a reminder of the importance of compliance checks on medical devices intended for the general public.

Radio Tripoint encourages its listeners and readers to consult the official information before using any of the products concerned.

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