Centurion Medical recalls GRIPPER Needles with Product Code DYNDC1582A due to supplier-initiated recall. Affected units include specific lot numbers and expiration dates.
Supplier initiated recall of the GRIPPER Needles
Centurion Medical is recalling GRIPPER Needles with Product Code DYNDC1582A. This supplier-initiated recall means the product may be unsafe, though the exact hazard isn't specified in the record.
The recall is initiated by the supplier, but the specific hazard is not described in the official notice. Without details on the hazard mechanism, it's unclear why the product is unsafe.
Patients using GRIPPER Needles for medical port access are likely affected. Healthcare providers who use these needles for medical procedures may also be at risk.
Check for Product Code DYNDC1582A on the needles. Affected units include specific lot numbers and expiration dates listed in the recall notice.
Look for Product Code DYNDC1582A on the needles to confirm if they are affected.
The recall is supplier-initiated, but the specific hazard is not described in the official notice.
Check the Product Code DYNDC1582A to see if your needles are affected. If they are, contact Centurion Medical for further instructions.
The official notice does not specify the hazard mechanism, so it's unclear if there are safety risks.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0255-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0255-2020 from Centurion Medical. 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.
