Synthes Spine N-Hance System 150 mm, Catalog number NH60150-1. spinal fusion surgery Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
N-Hance System 150 mm, Catalog number NH60150-1. spinal fusion surgery
Brand
Synthes Spine
Lot Codes / Batch Numbers
Lot number: P07M01 exp 12/31/08
Products Sold
Lot number: P07M01 exp 12/31/08
Synthes Spine is recalling N-Hance System 150 mm, Catalog number NH60150-1. spinal fusion surgery due to the dimensional specifications are incorrect. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
the dimensional specifications are incorrect
Recommended Action
Per FDA guidance
The recalling firm issued an e-mail on 11/18/08 to their sales force to inform them of the problem and the need to remove the product.The recalling firm issued Medical Device recall letters dated 11/19/08 to their customers to inform them of the problem and the need to return the product. Contact Synthes at 800-620-7025 ext. 7025 or 610-719-5750 for additional information.
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
AL, AK, AZ, AR, CA, CO, CT, FL, GA, IL, IN, KS, LA, MD, MA, MI, MN, MO, NV, NH, NJ, NM, NY, NC, ND, OH, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI
Page updated: Jan 10, 2026