Stryker recalls MOLLI 2 System surgical tools due to outdated labeling that may affect marker placement during procedures. Affected units include specific model numbers and serial ranges.
Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures.
Stryker is recalling certain MOLLI 2 System surgical tools because the product labeling needs updating. This update is required to prevent magnetized surgical markers from dislodging during tissue removal procedures.
The magnetized surgical markers in the MOLLI 2 System may dislodge during target tissue removal procedures if the product labeling is outdated. This could lead to inaccurate surgical site marking.
Medical professionals using the MOLLI 2 System for surgical procedures are likely affected. The risk is low as the issue relates to labeling updates rather than immediate safety hazards.
Check for the MOLLI 2 System with specific model numbers: MM1000 (Pack of 10), MS-00009 (Pack of 10), MP2001, MP2015A, and MT2001. Look for the provided serial number ranges in the recall notice.
Verify if your MOLLI 2 System has the updated labeling as required by the recall notice.
Stryker is recalling the MOLLI 2 System due to outdated labeling that may cause magnetized surgical markers to dislodge during tissue removal procedures.
No, the recall requires updating the labeling, not stopping use. The product can continue to be used with the updated instructions.
The affected models include MM1000 (Pack of 10), MS-00009 (Pack of 10), MP2001, MP2015A, and MT2001 with specific serial number ranges listed in the recall notice.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1427-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1427-2026 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.
