American Surgical Americot Blue Sponges Recalled for Packaging Defects
American Surgical Company is recalling 15 boxes of Americot Blue sponges because defective packaging compromises 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 involves a medical device where defective packaging compromises sterility, creating a risk of harm (infection) even though no specific injuries or illnesses are reported in the source text.
Plain-English summary
American Surgical Company is recalling 15 boxes of Americot Blue 3/8" x 2" sponges, reference number 20-26S. These neurosurgical and nonneurosurgical sponges were distributed worldwide, including in the United States and numerous international markets.
The recall was initiated because the product packaging is defective, which compromises the sterility of the sponges. The affected lot number is 2015/09 BJ.
Healthcare facilities and consumers should stop using these sponges and contact American Surgical Company for further instructions.
The recalled product
- Product
- American Surgical Americot Blue 3/8" x 2" Ref Number: 20-26S Product Usage: Neurosurgical and Nonneurosurgical Sponges
- Manufacturer
- American Surgical Company
- Hazard
- Affected units
- 15
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 BJ
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.
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