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Recall Observatory FDA recall evidence

Device product

Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion using autograft or allograft in skeletally mature patients.

Z-0270-2016

September 25, 2015

Class II

Product summary

Firm
Stryker Spine
Event
Event 72413
Status
Terminated
Classification
Class II
Quantity
42 units
Official record key
device-enforcement:Z-0270-2016

Official wording

Reason: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm (Catalog #486614530) because it does not have an associated 510(k) submisstion and subsequent clearance, which is required as this is a class 2 device.

Code information: Catalog #486614530, All Lots

Distribution pattern: Nationwide Distribution including the states of AK, AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, MT, NC, NM, NY, OH, OK, OR, PA, TN, TX, UT, WA and WI.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm (Catalog #486614530) because it does not have an associated 510(k) submisstion and subsequent clearance, which is required as this is a class 2 device.