The Recall Desk
HighFDA (Devices)·Z-1741-2016·Announced 2016-06-01

American Surgical Ultracot Sponges Recalled for Packaging Sterility Defect

American Surgical Company is recalling 39 boxes of Ultracot sponges because defective packaging may compromise sterility. The products were 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 medical device) where the defect may compromise sterility, but the source text does not report any injuries or illnesses, fitting the High severity criteria.

Plain-English summary

American Surgical Company is recalling 39 boxes of Ultracot 15 mm x 20 mm (Glassine) sponges, Reference Number 23-04G. These neurosurgical and nonneurosurgical sponges are being recalled because the product packaging is defective, which may compromise the sterility of the devices.

The affected lots are 2015/10 CJ, 2015/11 AC, and 2015/12 BQ. The products were distributed nationwide in the United States and internationally to Australia, Belgium, Canada, France, Germany, Greece, Hong Kong, Israel, Italy, Japan, Netherlands, New Zealand, Portugal, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and the United Kingdom.

Healthcare facilities and consumers should stop using these sponges and contact American Surgical Company for further instructions or a return.

The recalled product

Product
American Surgical Ultracot 15 mm x 20 mm (Glassine) Ref Number: 23-04G Product Usage: Neurosurgical and Nonneurosurgical Sponges
Affected units
39

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: 2015/10 CJ 2015/11 AC 2015/12 BQ

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 →