Aesculap recalls specific ELAN 4 Fixed Duraguard Long models due to mislabeling between standard and long versions. Affected units may be confused with incorrect product types.
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 specific ELAN 4 Fixed Duraguard Long models (model GB943R) because they were mislabeled as 'Long' when they should be 'Standard'. This could cause confusion about which product you have, but it doesn't pose a safety risk.
The mislabeling means the product might be confused with a different model (Standard vs. Long). This could lead to incorrect usage if the wrong product is selected, but it does not cause physical harm or injury.
Owners of the ELAN 4 Fixed Duraguard Long with model number GB943R and serial numbers 4519, 4528, or 4533 are affected. Medical device users who rely on precise labeling for correct product selection are most at risk.
Check for model number GB943R and serial numbers 4519, 4528, or 4533 on the product. The product is labeled as 'Long' but should be 'Standard' for this specific model.
Look for model number GB943R and serial numbers 4519, 4528, or 4533 to confirm if the product is affected.
No, this recall is due to mislabeling only, not a safety hazard. The product itself is safe but may be confused with the wrong model.
Check the product label for model number GB943R and serial numbers 4519, 4528, or 4533. If affected, you do not need to take action beyond verifying the model.
The affected product is labeled as 'Long' but should be 'Standard' for this specific model. Check the label for model number GB943R and serial numbers 4519, 4528, or 4533.
We’ve drafted a message you can send Aescul: Aesculap AG to request your refund or repair — edit it as you like.
Subject: Recall Z-0027-2026 — Aescul: Aesculap AG Aescul: Aesculap AG Hello, I own a Aescul: Aesculap AG that is covered by recall Z-0027-2026 from Aescul: Aesculap AG. 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.
