⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Is Aesculap recalled?

Aesculap recalls - full list & free alerts

Official U.S. agency records list 5 recalls involving Aesculap in the last 12 months, most recently on 2026-03-11. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

Recalls (5)

Aesculap Inc: Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product De
Medical DevicesFDA (device) · 2026-03-11 · Class II
Aesculap Inc: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Version: N/A Product D
Medical DevicesFDA (device) · 2025-11-05 · Class II
Aesculap Inc: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Model/Catalog Number: EK085P Software Version: N/A Product Descriptio
Medical DevicesFDA (device) · 2025-11-05 · Class II
Aesculap Inc: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Model/Catalog Number: EK086P Software Version: N/A Product Descripti
Medical DevicesFDA (device) · 2025-11-05 · Class II
Aesculap Inc: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A Product Descript
Medical DevicesFDA (device) · 2025-11-05 · Class II
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