PlainRecalls
FDA Devices Moderate Class II Ongoing

VA-LCP Clavicle Plate 2.7, shaft, CS1, right-Intended for fixation of clavicle bone fragments. Part Number: 02.112.621S

Reported: March 13, 2024 Initiated: January 24, 2024 #Z-1241-2024

Product Description

VA-LCP Clavicle Plate 2.7, shaft, CS1, right-Intended for fixation of clavicle bone fragments. Part Number: 02.112.621S

Reason for Recall

Products not sterilized, sterility cannot be confirmed

Details

Units Affected
47 units
Distribution
Worldwide distribution - US Nationwide and the countries of Argentina, Austria, Australia, Belgium, Canada, Czech Republic, Germany, Spain, Finland, France, United Kingdom, Ireland, South Korea, Kuwait, Mexico, Netherlands, Slovakia, Taiwan, South Africa.
Location
West Chester, PA

Frequently Asked Questions

What product was recalled?
VA-LCP Clavicle Plate 2.7, shaft, CS1, right-Intended for fixation of clavicle bone fragments. Part Number: 02.112.621S. Recalled by Synthes (USA) Products LLC. Units affected: 47 units.
Why was this product recalled?
Products not sterilized, sterility cannot be confirmed
Which agency issued this recall?
This recall was issued by the FDA Devices on March 13, 2024. Severity: Moderate. Recall number: Z-1241-2024.