Civco recalls reusable SonoSite needle guide brackets with specific reference numbers due to potential injury risk. Affected units include those with lot numbers A000012-A050663, M000880-M995980, and P022503.
See the official notice for the full hazard description.
Civco is recalling SonoSite needle guide brackets with reference numbers P06013-06 and P06013-07 because they may cause injury if used improperly. This recall affects medical professionals who use these brackets with SonoSite L25 transducers.
The recall states that brackets without proper labeling may be used incorrectly, leading to potential injury. However, the exact hazard mechanism is not clearly described in the notice.
Medical professionals using SonoSite L25 transducers with these brackets are most at risk. The recall applies to specific lot numbers and inventory units without current labeling.
Check for reference numbers P06013-06 or P06013-07 on the bracket. Affected units have lot numbers between A000012-A050663, M000880-M995980, or P022503, or brackets without current labeling.
Look for current product labeling on the bracket. If the bracket no longer has labeling, it is affected.
Check the lot numbers on the bracket box, which may be in the ranges A000012-A050663, M000880-M995980, or P022503.
The recall states that brackets without proper labeling may be used incorrectly, but the exact hazard mechanism is not clearly described.
Check for reference numbers P06013-06 or P06013-07, or lot numbers in the ranges A000012-A050663, M000880-M995980, or P022503. Affected brackets may also lack current labeling.
The recall does not specify a stop-use instruction, so you can continue using them if they have proper labeling and are within the listed lot numbers.
We’ve drafted a message you can send Civco Medical Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0566-2019 — Civco Medical Instruments Civco Medical Instruments Hello, I own a Civco Medical Instruments that is covered by recall Z-0566-2019 from Civco Medical Instruments. 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.
