Stryker recalls reprocessed HARMONIC Ace+7 shears that may show 'No Instrument Uses Remaining' error code, preventing use. Affected units may need replacement.
Stryker Sustainability Solutions has received an increase in reports indicating that the affected Reprocessed HARH36 devices may display an error code (No Instrument Uses Remaining) upon initial connection to the generator. When this error code is present, the device is not able to be used.
Stryker is recalling reprocessed HARMONIC Ace+7 shears that may display an error code when first connected to the generator, making them unusable. This affects medical devices used for precise cutting and hemostasis in surgeries.
The shears may show an error code (No Instrument Uses Remaining) after initial connection to the generator, which prevents them from being used. This could lead to incomplete procedures or potential complications during surgery.
Medical professionals using the reprocessed shears for surgical procedures are most at risk. Patients undergoing surgery with these devices could be affected if the error code prevents proper use.
Check for the product name 'HARMONIC Ace+7, 5mm Diameter Shears with Advanced Hemostasis (HARH)' and item number HARH36. The affected units were sold with lot number 7656512.
Look for the error code 'No Instrument Uses Remaining' when connecting the shears to the generator.
Stryker has received reports that the reprocessed shears may display an error code that prevents use after initial connection to the generator.
Check if the shears show the error code when connected to the generator. If so, stop using them and contact Stryker for further instructions.
The shears may not function properly, potentially leading to incomplete procedures or complications during surgery.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2484-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2484-2018 from Stryker. 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.
