Riverpoint Medical recalls 18G Brachy Grid (RPG-18) due to potential sterile packaging compromise. Affected units have specific lot numbers and UDI. Consumers should contact for details.
The integrity of the sterile grid packaging is potentially compromised.
Riverpoint Medical is recalling its 18G Brachy Grid (RPG-18) because the sterile packaging might be damaged. This could lead to contamination or infection if the device is used. The recall affects specific lot numbers and units with a unique identifier.
The sterile packaging might be damaged, which could lead to contamination. If the device is used without proper sterility, it might cause infection or other complications during medical procedures.
Medical professionals using the Riverpoint Medical 18G Brachy Grid for radiation therapy may be affected. Patients receiving treatment with this device are at risk if the packaging is compromised.
Check for the lot numbers listed: 16032422, 16051814, 16051815, 16052425, 17042430, 17050936, 17052532, 17061214, 17121823, 17122820, 18040922, 18061816, 18101521, and 18120705. The UDI number is 00812444028638.
Identify the lot numbers and UDI number on the device label to confirm if it is affected.
The recalled device is Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx.
Check for the lot numbers listed: 16032422, 16051814, 16051815, 16052425, 17042430, 17050936, 17052532, 17061214, 17121823, 17122820, 18040922, 18061816, 18101521, and 18120705. The UDI number is 00812444028638.
Contact Riverpoint Medical for instructions on how to handle the device. The recall does not specify a remedy.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0795-2020 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0795-2020 from Riverpoint 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.
