FDA recall record

Stryker Craniomaxillofacial Division MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm recall — FDA Z-1090-2015

Potential for implant damage, implant cracking off/breaking intra-operatively.

Class IIclassification
Z-1090-2015official record ID
Feb 18, 2015report date

Recall record at a glance

Official recordZ-1090-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmStryker Craniomaxillofacial Division
Report dateFeb 18, 2015
Recall initiation dateDec 17, 2014
Quantity1051
LocationPortage, MI, United States

Official product description

MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and MEDPOR BARRIER Implants are intended for the augmentation or restoration of bony contour in the craniofacial skeleton.

Why the product was recalled

Potential for implant damage, implant cracking off/breaking intra-operatively.

Distribution information

Worldwide Distribution - US Nationwide in the states of PA, KY, VA, CT, UT, MD, AR, FL, TX, AL, DE, IL, IA, MI, CO, OH, GA, CA, DC, MO, LA, WI, ID, SC, NC, NY, MA, NH, CA, OK, MN, KY, IN, OR, TN and the countries of: Argentina, Australia, Canada, Chile, China, Netherlands, France, Spain, South Korea, Colombia, Switzerland, Singapore, and 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: Letter.

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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