Aesculap recalls ELAN 4 Fixed Duraguard Standard (model GB942R) due to mislabeling between standard and long versions. Affected units may be confused with incorrect models.
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
Aesculap is recalling its ELAN 4 Fixed Duraguard Standard (model GB942R) because it was mislabeled as 'Long' when it should be 'Standard.' This confusion could lead to using the wrong product, but there's no immediate safety risk.
The product was mislabeled as 'Long' instead of 'Standard,' which could cause confusion with the longer version. This might lead to incorrect usage in medical procedures, but the recall does not indicate any immediate safety hazard.
Users of the ELAN 4 Fixed Duraguard Standard (model GB942R) who may have confused it with the ELAN 4 Fixed Duraguard Long. Medical professionals using this product are most at risk of using the wrong model.
Check for model number GB942R or serial number 8157 on the product. The product was labeled as 'Long' but should be 'Standard' to identify the correct version.
Look for the model number GB942R or serial number 8157 to confirm you have the recalled item.
No, the recall is due to mislabeling, not a safety hazard. There is no risk of injury from using the product correctly.
Check for model number GB942R or serial number 8157 on the product. The product was labeled as 'Long' but should be 'Standard' to identify the correct version.
The recall does not require returning the product; it's a mislabeling issue that needs correction through proper identification.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-0026-2026 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-0026-2026 from Aesculap. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
