Haemonetics recalls OrthoPAT System-Integrated Set (Product Code 1150H-00) due to missing cannula in reservoirs, preventing blood from being processed. Affected units sold with Lot #1017049 and 1150H-00.
OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The absence of this cannula prevents the emptying of blood from the reservoirs. The inability to empty the reservoir means that the collected blood cannot be processed.
Haemonetics is recalling its OrthoPAT System-Integrated Set because the reservoirs lack a critical cannula. Without this component, blood collected during surgery cannot be processed, risking potential complications for patients.
The reservoirs in the OrthoPAT system are missing the cannula that normally allows blood to be emptied. Without this cannula, the collected blood cannot be processed, which could lead to complications during surgery or recovery.
Surgical teams and hospitals using the OrthoPAT System-Integrated Set with Product Code 1150H-00 are affected. Patients undergoing surgery with this system are at risk of complications due to improper blood processing.
Check for the Product Code 1150H-00 on the OrthoPAT System-Integrated Set. Units sold with Lot numbers 1017049 and 1150H-00 are affected.
Inspect the reservoirs for the presence of the cannula; if missing, the unit is affected.
The OrthoPAT reservoirs are missing the cannula inside, which prevents blood from being emptied and processed.
Check if the reservoirs have the cannula; if missing, contact Haemonetics for guidance.
The recall record does not specify a remedy, so contact Haemonetics directly for assistance.
We’ve drafted a message you can send Haemonetics to request your refund or repair — edit it as you like.
Subject: Recall Z-2950-2018 — Haemonetics Haemonetics Hello, I own a Haemonetics that is covered by recall Z-2950-2018 from Haemonetics. 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.
