Every recall we track for TriMed Inc. — 18 in all — plus the complaints and injury reports the public filed about them.
TriMed recalls 3.6mm threaded IM nails with a driver-socket that may not apply sufficient torque, risking improper use. Affected items have specific model numbers and lot codes.
TriMed recalls 3.6mm threaded IM nails with a driver-socket that may not hold properly, risking improper use. Affected items have specific model numbers and lot codes.
TriMed recalls specific Volar Bearing Plate models used in wrist surgery due to risk of bearings popping out of distal peg holes during procedures.
TriMed recalls RipCord Syndesmosis Button REF STA001K due to risk of button breaking during surgery, potentially causing complications. Affected units have UDI-DI 00842188123849 and Lot 85305-0: stop using immediately.
TriMed recalls two wrist hook impactors (WHD/WHV) due to potential rust from improper manufacturing. Affected units have specific lot numbers and were sold with nonsterile labels. Consumers should check their product details.
TriMed recalls Hex Driver 1.2 surgical tools due to epoxy coating that may pop off. Affected models include HXDRIVR-1.2C AO with specific lot numbers. No remedy stated in recall notice.
TriMed recalls 2.3mm Locking Drill Guides with epoxy that may pop off. Affected units have specific lot numbers. Stop using immediately to avoid injury.
TriMed recalls Peg Guide Extenders (REF PEG-XTNDR) due to potential rust from steel spring. Nonsterile, prescription-only device. Check lot numbers 2858, 2861, 3749 for affected units.
TriMed recalls 1.7mm Countersink instruments due to epoxy coating that may pop off. Affected items have lot number 91401455. Stop using immediately to prevent injury.
TriMed recalls Hex Cortical Screw 4.0, 40mm (REF HEX4.0-40) due to being shorter than intended. This component of ankle fixation systems may not properly secure fractures during healing.
TriMed recalls Dorsal Wrist Hook Plate model WHD-4 due to potential structural issues from design control process failures. Affected units include specific lot numbers sold in Santa Clarita, CA.
TriMed recalls specific olecranon hook plates due to potential unqualified modifications to angled holes, which may affect bone fixation safety. Affected units include Lot #110631.
TriMed recalls UOCP-S ulnar osteotomy plates with misaligned saw guide holes. These plates are non-sterile and used in ulna osteotomy procedures. Affected units have lot numbers 10003 or 10017.
TriMed recalls specific nitinol staple models due to potential patient infection risks from improper sterilization records. Affected lots include ES-08x08 through ES-15x12 with various lot numbers. Consumers should contact TriMed for details.
TriMed recalls specific Nitinol staples due to potential sterilization failures that could cause patient infections. Affected lots include ES-18x15x17 and ES-18x17x19 models with certain lot numbers.
TriMed recalls specific Nitinol elastic staples due to potential patient infection risks from improper sterilization records. Affected lots include ES-18x14, ES-20x20, and ES-25x22 models with certain lot numbers.
TriMed recalls specific Nitinol staple models due to potential sterilization failures that could cause patient infections. Affected lots include ES-10x13x15 and other sizes with listed lot numbers. Consumers should contact TriMed for details.
TriMed recalls specific Hex Driver models due to epoxy band migration after sterilization cycles, potentially contaminating trays. Affected units include HXDRIVER-2.0 AO, HXDRIVR-2.5 AO, and others with listed lot numbers.
