The Recall Desk
HighFDA (Devices)·Z-2047-2014·Announced 2014-07-23

Smith & Nephew Recalls SUTUREFIX Ultra S Devices Due to Sterility Breach

Smith & Nephew is recalling 907 units of SUTUREFIX Ultra S devices because a breach in the sterile barrier compromises the device's sterility.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II. The hazard involves a compromised sterile barrier, which poses a risk of infection (risk-of-harm), but the source text does not report any specific illnesses or injuries, placing it in the High severity category per the rubric.

Plain-English summary

Smith & Nephew, Inc. Endoscopy Division is recalling 907 units of SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) (Product Code: 72203852). The recall is being conducted because the sterility of the device is compromised due to a breach in the sterile barrier.

The affected products are nondegradable soft tissue fasteners. The recall covers specific lot numbers: 50478982, 50478985, 50482873, 50485588, 50486705, 50486707, 50491897, and 50491899.

The products were distributed nationwide in the United States and internationally to Australia, Belgium, Denmark, France, Germany, Great Britain, Italy, Netherlands, Norway, Portugal, Spain, and Sweden. Users should stop using the affected devices and contact the manufacturer for further instructions.

The recalled product

Product
SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: 72203852 Fastener, fixation, nondegradable, soft tissue
Manufacturer
Smith & Nephew, Inc. Endoscopy Division
Category
Medical Device — Surgical Fasteners
Hazard
Affected units
907

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (8)

  • Lot Numbers: 50478982
  • 50478985
  • 50482873
  • 50485588
  • 50486705
  • 50486707
  • 50491897
  • 50491899

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 5 recalled by Smith & Nephew, Inc. Endoscopy Division under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 5 products in this recall →

Related recalls

Same manufacturer · Smith & Nephew, Inc. Endoscopy Division

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Same hazard · sterility breach

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