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Serious recall: Injury is possible or has been reported. Take action promptly.

Synthes (USA) Products LLC 2024-03-13 Health serious FDA
Health · FDA · Recall #FDA-Z-1238-2024

RAPIDSORB IPS Battery Pack, Sterile-Intended for use in non-load bearing fracture repair… Recall

Issued March 13, 2024 · Synthes (USA) Products LLC

In March 2024, Synthes (USA) Products LLC recalled the RAPIDSORB IPS Battery Pack, Sterile-Intended for use in non-load bearing fracture repair…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Products not sterilized, sterility cannot be confirmed

What you should do

  1. 1 Stop using RAPIDSORB IPS Battery Pack, Sterile-Intended for use in non-load bearing fracture repair… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Synthes (USA) Products LLC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Synthes (USA) Products LLC
Category
Health
Recall date
March 13, 2024
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide and the countries of Argentina, Austria, Australia, Belgium, Canada, Czech Republic, Germany, Spain,
Recall number
FDA-Z-1238-2024
Made in
United States
Issuing agency
FDA

In context

  • Synthes (USA) Products LLC has 5 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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