Product Wiki · Recalls · UK OPSS (Office for Product Safety and Standards)

Black diamond equipment neve strap crampons green 2024 version — recall 2405-0119

UK OPSS (Office for Product Safety and Standards) · GB · 2024-06-13 · Product Recall

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
UK OPSS (Office for Product Safety and Standards)
Recall identifier
product-recall-black-diamond-equipment-neve-strap-crampons-green-2024-version-2405-0119
Date of alert
2024-06-13
Country / jurisdiction
GB
Authority classification
Product Recall
Risk type
product-recall
Brand
Black Diamond Equipment
Product category
personal-protective-equipment-ppe
Reported risk: The product presents a high risk of injuries as the screws which connect the plastic heel cup to the aluminium heel unit of the Neve Strap Crampon can loosen. This could result in the heel cup detaching from the crampon, posing a fall or injuries hazard. The product does not meet the requirements of the Regulation (EU) 2016/425 on Personal Protective Equipment or the Personal Protective Equipment (Enforcement) Regulations 2018.
What to do

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from UK OPSS (Office for Product Safety and Standards) →

Primary source: https://www.gov.uk/product-safety-alerts-reports-recalls/product-recall-black-di

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.