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Recall Observatory FDA recall evidence

Device product

1. InterPulse Handpiece with coaxial bone cleaning tip, Product Number: 0210-110-100, UDI: (01)4546540861641; 2. InterPulse Handpiece with Coaxial High Flow Tip, Product Number: 0210-114-100, UDI: (01)4546540861764; 3. InterPulse Handpiece with Retractable Coaxial Fan Spray Tip, Product Number: 0210-118-200, UDI: (01)4546540861818; 4. InterPulse Irrigation Only Handpiece with Fan Spray Tip, Product Number: 0210-218-000, UDI: (01)4546540144300 for orthopedic use.

Z-1246-2018

November 09, 2017

Class II

Product summary

Firm
Stryker Instruments Div. of Stryker Corporation
Event
Event 79418
Status
Terminated
Classification
Class II
Quantity
5988
Official record key
device-enforcement:Z-1246-2018

Official wording

Reason: Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates.

Code information: 1. Lot Numbers: 17283012, 17284012, 17286012; 2. Lot Numbers: 17278012, 17280012, 17282012, 17283012, 17285012, 17289012, 17292012; 3. Lot Number: 17279012; 4. Lot Number: 17284012 UDI: (01)4546540861641; (01)4546540861764; (01)4546540861818; (01)4546540144300

Distribution pattern: Distributed in all 50 U.S. States and the District of Columbia. Distributed in Australia, Argentina, Japan, Canada, Chile, Korea, Spain, France, Italy, Netherlands, and United Kingdom.

Derived failure modes

  • Microbial contamination

    reason.microbial_contamination · v1.0.0

    bioburden levels were found
  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    Lack of sterility