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[Recalled] Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm Catalog Number: 18965037S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones. — Seal integ

recall fda device switzerland

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductStryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm Catalog Number: 18965037S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
Brand / manufacturerStryker GmbH
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2383-2020
Country of noticeSwitzerland
Risk levelClass II
Hazard typerecall
Notice date07 May 2020

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Seal integrity of the blister pack may be compromised and sterility cannot be assured

This Class II recall concerns device products distributed in Switzerland and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Stryker GmbH

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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