FDA recall record

Synthes (USA) Products RIA Tube Assembly, minimum 520 mm length, sterile- intended for use recall — FDA Z-1237-2024

Products not sterilized, sterility cannot be confirmed

Class IIclassification
Z-1237-2024official record ID
Mar 13, 2024report date

Recall record at a glance

Official recordZ-1237-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSynthes (USA) Products LLC
Report dateMar 13, 2024
Recall initiation dateJan 24, 2024
Quantity144 units
LocationWest Chester, PA, United States

Official product description

RIA Tube Assembly, minimum 520 mm length, sterile- intended for use in adults and adolescents (12-21 years) to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary implant or prosthesis, to harvest finely morselized autogenous bone and bone marrow for any surgical procedure requiring bone graft to facilitate fusion and/or fill bone defects, and to remove infected and necrotic bone and tissue from the medullary canal in the treatment of osteomyelitis. Part Number: 314.746S

Why the product was recalled

Products not sterilized, sterility cannot be confirmed

Distribution information

Worldwide distribution - US Nationwide and the countries of Argentina, Austria, Australia, Belgium, Canada, Czech Republic, Germany, Spain, Finland, France, United Kingdom, Ireland, South Korea, Kuwait, Mexico, Netherlands, Slovakia, Taiwan, South Africa.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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