Klarity Medical Products recalls vacuum bags used in radiation therapy that may not hold vacuum properly, risking patient treatment safety. Affected items include specific model numbers and lot codes.
Vacuum bags potentially may not hold their vacuum adequately for needed patient treatment times.
Klarity Medical Products is recalling vacuum bags used in radiation therapy treatment that might not hold vacuum adequately during patient procedures. This could lead to improper patient positioning and treatment risks if the bags fail.
The vacuum bags may not maintain sufficient vacuum pressure for the required duration of patient treatment. This could cause improper positioning of the patient, potentially affecting the effectiveness of radiation therapy and increasing the risk of complications.
Medical professionals using these vacuum bags in hospitals or clinics for radiation therapy patients. Patients receiving treatment with these bags are at risk if the bags fail during procedures.
Check for model numbers R7504-30C, R7504-35BC, R7504-35C, R7644-32.5BC, RC7221-25BC, or RC7504-17.5C. Also look for specific lot codes listed in the recall notice.
Identify the model number and lot code on the vacuum bag to confirm if it is affected.
The vacuum bags may not hold their vacuum adequately for needed patient treatment times, which could lead to improper patient positioning during radiation therapy.
Check the model number and lot code to see if it is affected. If it is, contact Klarity Medical Products for further instructions.
The recall indicates a potential risk, so affected units should be checked and handled according to the manufacturer's instructions to ensure patient safety.
We’ve drafted a message you can send Klarity to request your refund or repair — edit it as you like.
Subject: Recall Z-2881-2020 — Klarity Klarity Hello, I own a Klarity that is covered by recall Z-2881-2020 from Klarity. 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.
