The FDA has posted 24 enforcement recalls of intramedullary and accessories fixation rod devices since 2025, none of them Class I (most serious). Most recent report: Jun 24, 2026.
Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before implantation, an equivalent backup can be used, or a bent na…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.…
Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Rod, Fixation, Intramedullary And Accessories”). Informational only — verify against the FDA before acting.