Reported Nov 4, 2026 · Ongoing
Precision Pointer Electromagnetic (8000-050-001)
Stryker Leibinger GmbH & Co. KG
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Leibinger GmbH & Co. KG · Botzinger Str. 39-41 · Freiburg Im Breisgau
Is this the product you have?
- Precision Pointer Electromagnetic (8000-050-001)
- Lot codes and dates
- Lot 7000413361 UDI-DI 07613327413205
- Amount recalled
- 513
Where it was sold
Why it was recalled
Device may fracture during use at the laser welded joint on the pointer tube. If this happens, loose parts may fall out of the product while the device is inside the patient.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Stryker Leibinger GmbH & Co. KG recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.