Deerfield Imaging recalls ORT300 operating room tables with serial numbers 10002255-10005613. The rotational locking mechanisms may fail to lock, causing unintended movement during procedures.
The rotational locking mechanisms on the ORT 200/300 tables fail to operate such that it cannot change states between locked and unlocked.
Deerfield Imaging is recalling ORT300 operating room tables that have a risk of failing to lock properly. This could lead to unintended movement during medical procedures, potentially causing injury.
The rotational locking mechanisms may not function correctly, preventing the table from securely locking between locked and unlocked states. This could cause unintended movement during medical procedures, potentially leading to injury.
Medical facilities using the ORT300 tables with the listed serial numbers are affected. Patients and staff at these facilities are at risk during procedures if the table fails to lock.
Check the serial numbers listed: 10002255, 10002841, 10002996, 10002997, 10002998, 10004372, 10004515, 10005456, 10005612, 10005613, 10005695, 10007377, 10007411. The tables are used in operating rooms for surgical procedures.
Ensure the table locks securely before use. If it fails to lock, stop using it immediately.
The rotational locking mechanisms may fail to operate correctly, causing the table to not lock between locked and unlocked states.
Serial numbers: 10002255, 10002841, 10002996, 10002997, 10002998, 10004372, 10004515, 10005456, 10005612, 10005613, 10005695, 10007377, 10007411.
The recall states the locking mechanism may fail, but the remedy is not specified. Check the locking mechanism before use; if it fails, stop using it immediately.
We’ve drafted a message you can send Deerfield Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-1218-2018 — Deerfield Imaging Deerfield Imaging Hello, I own a Deerfield Imaging that is covered by recall Z-1218-2018 from Deerfield Imaging. 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.
