Cypress Medical Products recalls 241-McKesson Premium Skin Staple Remover Kit and related items due to iodine assay levels not meeting 36-month expiration requirements. Consumers should contact the manufacturer for details.
Product not meeting the iodine assay level requirements to support 36 month expiration dating.
Cypress Medical Products is recalling certain skin staple remover kits because they don't meet iodine assay standards needed for safe 36-month expiration dating. This means the products could expire before the intended use period, potentially affecting medical safety.
The kits fail to meet iodine assay requirements, which are necessary for the product to remain safe and effective for 36 months. This could lead to expiration before the intended use period, potentially affecting medical safety.
Healthcare professionals and medical facilities using the recalled kits are most at risk. The recall applies to specific kits sold through McKesson.
Check for the product names: 241-McKesson Premium Skin Staple Remover Kit (Item #100123), McKesson I.V. Start Kit (Item #100124), or Cypress Skin Staple Remover Kit (Item #82-15). These were sold through McKesson.
Reach out to Cypress Medical Products for specific instructions on handling the recalled items.
The kits do not meet iodine assay requirements needed for 36-month expiration dating.
241-McKesson Premium Skin Staple Remover Kit (Item #100123), McKesson I.V. Start Kit (Item #100124), and Cypress Skin Staple Remover Kit (Item #82-15).
Look for the product names and item numbers listed in the recall notice.
We’ve drafted a message you can send Cypress Medical Products to request your refund or repair — edit it as you like.
Subject: Recall Z-0932-2018 — Cypress Medical Products Cypress Medical Products Hello, I own a Cypress Medical Products that is covered by recall Z-0932-2018 from Cypress Medical Products. 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.
