TriMed recalls two wrist hook impactors (WHD/WHV) due to potential rust from improper manufacturing. Affected units have specific lot numbers and were sold with nonsterile labels. Consumers should check their product details.
The WHD/WHV impactors can rust over time due to an improper manufacturing process.
TriMed is recalling two types of wrist hook impactors (WHD and WHV) because they can rust over time due to a manufacturing defect. This rust risk may lead to the device becoming unsafe or unusable, but the recall does not mention injuries or immediate danger.
The impactors can rust over time because of an improper manufacturing process. Rust may cause the device to become unsafe or unusable, but the recall does not indicate a risk of injury or serious harm in normal use.
People who own or use the TriMed Wrist Hook Dorsal Impactor (REF IMPCT-WHD) or Volar Impactor (REF IMPCT-WHV) with lot numbers 049044, 049045, or 049044R1 are affected. Those using these devices for medical purposes are most at risk due to potential rust issues.
Check for the product name 'TriMed Wrist Hook Dorsal Impactor' or 'Volar Impactor' with lot numbers 049044, 049045, or 049044R1. These devices were sold with nonsterile labels and manufactured by TriMed Inc. in Santa Clarita, CA.
Look for the lot numbers 049044, 049045, or 049044R1 on the device label to confirm if it is affected.
The recall states the devices can rust over time due to a manufacturing defect, but does not indicate they are unsafe in normal use. They are nonsterile and intended for medical use.
Check the lot number on the device label. If it matches 049044, 049045, or 049044R1, contact TriMed Inc. for further instructions.
The recall does not mention any risk of injury from rust. The hazard is limited to potential rust causing the device to become unsafe or unusable.
We’ve drafted a message you can send TriMed to request your refund or repair — edit it as you like.
Subject: Recall Z-0359-2020 — TriMed TriMed Hello, I own a TriMed that is covered by recall Z-0359-2020 from TriMed. 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.
