Exactech, Inc. AcuMatch M-Series Straight Fluted Stem Segment and AcuMatch M-Series Curved Fluted Stem Segment. Catalog numbers 150-07-19 and 150-07-44. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AcuMatch M-Series Straight Fluted Stem Segment and AcuMatch M-Series Curved Fluted Stem Segment. Catalog numbers 150-07-19 and 150-07-44.
Brand
Exactech, Inc.
Lot Codes / Batch Numbers
0797860, 0797861, 0797862, 0797857, 0797858, 0797859
Products Sold
0797860, 0797861, 0797862, 0797857, 0797858, 0797859
Exactech, Inc. is recalling AcuMatch M-Series Straight Fluted Stem Segment and AcuMatch M-Series Curved Fluted Stem Segment. Cat due to The packaging was mislabeled: Exterior and interior packaging on the device was labeled with catalog number 150-07-19 15mm x 200mm, however, the act. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The packaging was mislabeled: Exterior and interior packaging on the device was labeled with catalog number 150-07-19 15mm x 200mm, however, the actual part inside the packaging was a 21mm x 200mm (catalog number 150-07-44) device.
Recommended Action
Per FDA guidance
The consignees were contacted by fax and email (dated July 21, 2006) to inform them of the recall requesting return of product
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
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Page updated: Jan 10, 2026