Medical device recalls Moderate risk

Synthes (USA) Products LLC recalls 2.5 mm Reaming Rod, Ball tip with extension, 950 mm, sterile, Part Number: 351.707S Reaming Rods are intended for guidi…

Recall date
July 26, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0902-2018
FDA classification
Class II
Brand / firm
Synthes (USA) Products LLC
Sold / distributed
Worldwide Distribution: US (Nationwide) to states of: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, the District of Columbia, including Puerto Ri…

Why it was recalled

Possible lack of product sterility due to potential gaps/channeling in the seal of the package.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

2.5 mm Reaming Rod, Ball tip with extension, 950 mm, sterile, Part Number: 351.707S Reaming Rods are intended for guiding of reamers during orthopedic surgery.

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