Aesculap Implant Systems LLC recalls Strauss Penis Clamp 130MM/General Instruments
- Recall date
- February 16, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1359-2018
- FDA classification
- Class III
- Brand / firm
- Aesculap Implant Systems LLC
- Sold / distributed
- nationwide
Why it was recalled
The plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Strauss Penis Clamp 130MM/General Instruments
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