FDAJune 22, 2018device
QUIKFLAP, 3 X 2-HOLE PLATES WITH TAB, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01532S, for use on the cranium
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
What to do
FDA enforcement status: Terminated
Brands named
stryker leibinger gmbh co kgstrykerstryker leibinger
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDAPediatric care bed; Product Designation: KayserBett IDA;2026-05-04
- FDADaig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic Tip Steerable, Product Number 6DYNTP001;2026-04-10
- FDABW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
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