ROi CPS LLC recalls ortho surgery convenience kits containing 3M surgical drapes due to potential safety concerns. Affected items include model OR00123Z with item number 880118026.
Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
ROi CPS LLC has recalled ortho surgery convenience kits that include 3M surgical drapes. The recall is due to the drapes being part of a previously recalled product line, though the specific hazard isn't detailed in the notice.
The recall involves surgical drapes that were previously distributed as part of a product line that was later recalled. The specific hazard mechanism is not clearly described in the notice, so the risk level cannot be determined.
Orthopedic surgeons and medical facilities that purchased the affected ortho surgery convenience kits are likely affected. Patients using these kits during procedures may be at risk if the drapes are used improperly.
Check for the model number OR00123Z and item number 880118026 on the kit. The affected kits were sold with lot number 92274 and expire May 2, 2024.
Identify the model number OR00123Z and item number 880118026 on the ortho surgery convenience kit.
The recall involves surgical drapes that were part of a previously recalled product line, but the specific hazard is not clearly described in the notice.
Check the model number and item number on the kit to see if it matches the affected items. The recall notice does not specify a remedy.
The recall notice does not describe a specific hazard mechanism, so the risk level cannot be determined.
We’ve drafted a message you can send ROi CPS LLC to request your refund or repair — edit it as you like.
Subject: Recall Z-0307-2023 — ROi CPS LLC ROi CPS LLC Hello, I own a ROi CPS LLC that is covered by recall Z-0307-2023 from ROi CPS LLC. 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.