Hydrocision, Inc. HydroCision SpineJet XL MIS 20 degree Handpieces, for cutting, ablation, and removal of soft tissue, hard tissue, and bone. Catalog Number 58662 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HydroCision SpineJet XL MIS 20 degree Handpieces, for cutting, ablation, and removal of soft tissue, hard tissue, and bone. Catalog Number 58662
Brand
Hydrocision, Inc.
Lot Codes / Batch Numbers
Lot Number 75GF2531
Products Sold
Lot Number 75GF2531
Hydrocision, Inc. is recalling HydroCision SpineJet XL MIS 20 degree Handpieces, for cutting, ablation, and removal of soft tissue, due to Distal tip may become detached from the device. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Distal tip may become detached from the device
Recommended Action
Per FDA guidance
Hydrocision contacted customers and sales reps by email on 9/6/06 advising to users to discontinue use and return recalled units.
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 noticePage updated: Jan 10, 2026