Zimmer Inc. Zimmer Spine Cyclone anterior cervical plate, 1 Level, 14MM (Ti-6Al-4V); REF 600-01-114. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer Spine Cyclone anterior cervical plate, 1 Level, 14MM (Ti-6Al-4V); REF 600-01-114.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
All lots.
Products Sold
All lots.
Zimmer Inc. is recalling Zimmer Spine Cyclone anterior cervical plate, 1 Level, 14MM (Ti-6Al-4V); REF 600-01-114. due to The screw locking cap may fracture when the surgeon rotates it into the locked position.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The screw locking cap may fracture when the surgeon rotates it into the locked position.
Recommended Action
Per FDA guidance
Consignees were notified via voicemail on 3/26/08 and a letter was sent to all distributors on 3/27/08 informing them that the plate should no longer be used and that all lots are being recalled. A letter dated 6/18/08 was issued to implant physicians recommending patient monitoring. Contact Zimmer Spine at 1-952-857-5636 for assistance.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, FL, GA, LA, MI, MN, MT, NH, NC, OK, PA, TN, TX, UT, WA, WI
Page updated: Jan 10, 2026