ROi recalls surgical packs labeled 'LAP - FLOL LADY OF ANGELS' with specific Stryker tube sets that may detach, causing gas leaks or hissing sounds. Affected units include model numbers 0620 040 and related parts.
Resource Optimization & Innovation (ROi) has received a recall notice from Stryker regarding tube sets potentially detaching from the cassette, which can lead to leaking gas or a hissing sound.
ROi is recalling surgical packs labeled 'LAP - FLOL LADY OF ANGELS' that include Stryker tube sets which may detach from the cassette. This could lead to gas leaks or a hissing sound, posing a risk during medical procedures.
The tube sets can detach from the cassette, potentially causing gas leaks or a hissing sound. This could disrupt the medical procedure and lead to unsafe conditions if not addressed promptly.
Surgical teams using the recalled packs are most at risk, particularly during procedures requiring precise gas management. Patients and staff using these packs in hospitals or clinics may be affected.
Check for surgical packs labeled 'LAP - FLOL LADY OF ANGELS' with Stryker part numbers 0620 040, 0620 040 660, 0620 040 690, or 0620 040 680. The item numbers include specific lot codes like 800096004 and 800096005.
Inspect the tube sets for signs of detachment from the cassette, which may cause gas leaks or a hissing sound.
The recalled Stryker tube sets include part numbers 0620 040 660 Pneumosure High Flow II Tubeset, 0620 040 690 Pneumosure Heated Tubeset with RTP, and 0620 040 680 Pneumosure High Flow Tubeset with RTP.
Check for the label 'LAP - FLOL LADY OF ANGELS' and Stryker part numbers 0620 040 or related items with specific lot codes like 800096004 or 800096005.
The recall does not require immediate stop use; however, check for detachment and address any signs of gas leaks or hissing sounds.
We’ve drafted a message you can send ROi to request your refund or repair — edit it as you like.
Subject: Recall Z-2220-2019 — ROi ROi Hello, I own a ROi that is covered by recall Z-2220-2019 from ROi. 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.
