The Recall Desk
HighFDA (Devices)·Z-1806-2016·Announced 2016-06-01

American Surgical Telfa Sponges Recalled for Packaging Sterility Defect

American Surgical Company is recalling Telfa 1" x 3" sponges because defective packaging compromises sterility. The recall covers 57 boxes distributed worldwide.

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 involves a risk-of-harm product (sterile surgical sponges) where the defect compromises sterility, but no injuries or illnesses have been reported in the source text.

Plain-English summary

American Surgical Company is recalling 57 boxes of Telfa 1" x 3" sponges, Reference Number 80-13, used for neurosurgical and nonneurosurgical procedures. The recall is due to defective product packaging that compromises the sterility of the sponges.

The affected products are identified by lot numbers 2015/08 BS and 2015/12 AR. These sponges were distributed nationwide in the United States and internationally to Australia, Belgium, Canada, France, Germany, Greece, Hong Kong, Israel, Italy, Japan, the Netherlands, New Zealand, Portugal, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and the United Kingdom.

Consumers and healthcare facilities should stop using the affected sponges and contact American Surgical Company for further instructions.

The recalled product

Product
American Surgical Telfa 1" x 3" Ref Number: 80-13 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Affected units
57

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 (1)

  • Lot numbers: 2015/08 BS 2015/12 AR

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 91 recalled by American Surgical Company 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 91 products in this recall →