Z-1944-2015 Class II Terminated

Recalled by Biomet, Inc. — Warsaw, IN

FDA device recall Z-1944-2015 was initiated by Biomet, Inc. on Jun 3, 2015 and is designated Class II. Reason for recall: Part Number: 905620 Lot: 824610 Gentle Threads Interference Screw 10x25mm Round Head is mixed with the Part Number: 905627 Lot: 753410 Gentle Threads Interference Screw 9x35mm Full Thread. If the… The recall status is terminated (terminated Dec 22, 2015). Affected quantity: 53 units.

Recall Details

Product Type
Devices
Report Date
Jul 8, 2015
Initiation Date
Jun 3, 2015
Termination Date
Dec 22, 2015
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
53 units

Product Description

Gentle Threads Interference Screw 10x25mm Round Head. An interference fixation screw for use in soft tissue reattachment procedures.

Reason for Recall

Part Number: 905620 Lot: 824610 Gentle Threads Interference Screw 10x25mm Round Head is mixed with the Part Number: 905627 Lot: 753410 Gentle Threads Interference Screw 9x35mm Full Thread. If the incorrect screw is used various failures may occur which may ultimately lead to revision surgery or a delay in surgery.

Distribution Pattern

Distribution-Domestic: None. International: Australia, Mexico, Chile, Costa Rica, Netherlands, and Brazil.

Code Information

Part Number: 905620 Lot: 824610

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1944-2015
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.