The Recall Desk
HighFDA (Devices)·Z-1809-2016·Announced 2016-06-01

American Surgical Policot Sponges Recalled for Packaging Sterility Defect

American Surgical Company is recalling Policot sponges because defective packaging compromises 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 is classified as FDA Class II and involves a risk-of-harm product (sterility compromise) where injury has not yet been reported, meeting the criteria for a High severity score.

Plain-English summary

American Surgical Company is recalling 4 boxes of Policot 1/2" x 1.5" sponges (Ref Number: 90-08) due to defective packaging that compromises sterility. These neurosurgical and nonneurosurgical sponges were distributed worldwide, including in the United States, 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.

The recall is limited to lot number 2015/09 BA. The FDA has classified this as a Class II recall. The source text does not report any specific illnesses or injuries associated with this defect.

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

The recalled product

Product
American Surgical Policot 1/2" x 1.5" Ref Number: 90-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Affected units
4

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: 2015/09 BA

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 →