Acumatch L-Series BP-2844Recalls & reported problems
Exactech, Inc. · Class 2 · Implant
All models of Acumatch L-Series (9)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862104939), received between Jan 15, 2020 and Jan 15, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Naturally Worn” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Naturally Worn1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 15, 2020Naturally Worn; Naturally Worn
AS REPORTED, THIS (B)(6) Y/O ACTIVE FEMALE EXPERIENCED A IMPLANTATION OF THE FEMORAL HEAD REPLACEMENT FOR LEFT FEMORAL NECK FRACTURE WAS PERFORMED USING NOVATION TAPERED STEM, BIPOLAR CUP, AND METAL HEAD ON (B)(6) 2014. THE PATIENT IS NOW UNDERGOING A RIGHT TOTAL HIP ARTHROPLASTY REVISION DUE TO PROXIMAL MIGRATION OF THE BIPOLAR CUP WAS OBSERVED BY X-RAY REVIEW. THE PROCEDURE WAS ON (B)(6) 2019 AT POST-OPERATIVE 5-YEARS AND 9-MONTHS. AT THE TIME OF THE RE-OPERATION, THE BIPOLAR CUP AND THE METAL HEAD WAS REMOVED BUT A REMARKABLE DELAMINATION WEAR THAT MIGHT BE CAUSED BY OXIDATION WAS OBSERVED AROUND THE LOCKING RING OF THE POLYETHYLENE BIPOLAR LINER. PATIENT¿S WEIGHT (B)(6) LBS, HEIGHT 4¿7¿. DEVICES ARE TO BE RETURNED FOR INVESTIGATION.
Patient problems: Failure of Implant
MAUDE report 9591528 ↗
Other Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented devices
- STAGEONE 431209Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 recalls0 reports
- SELF CENTERING 1035-45-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented84 reports
- LFIT 6260-9-036Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented80 reports
- ACTIS 101011060Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented66 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165228Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall1 death12 reports
- SELF CENTERING 1035-44-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented60 reports
- TANDEM 71324046Smith & Nephew, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall9 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145170Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented59 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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