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SIDEKICK

WRIGHT MEDICAL TECHNOLOGY, INC. · Model RR3520180TN · UDI-DI 00840420128423

HTY JEC KTT Prescription

510(k) clearances

2,868

Adverse events (1 deaths)

Recalls

280

Facilities

Recalls

Date	Firm	Reason
2026-06-23	Arrowhead DE LLC	Implant indicated for fixation of osteotomies, arthrodeses and reconstruction in the lesser toes following corrective procedures, did not undergo required gamma radiation dose audi
2024-07-09	Smith & Nephew, Inc.	Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contain
2024-07-09	Smith & Nephew, Inc.	Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contain
2022-05-26	Paragon 28, Inc.	Due to Titanium plasma coating not present implant.
2022-03-28	Stryker GmbH	The nickel-sensitivity statement on the outer carton may be partially covered by a label resulting in the statement showing "Indicated for patients with Nickel sensitivity" instead
2022-01-28	Brasseler USA, Medical L.L.C.	One lot of product was distributed in unsealed packaging
2019-12-11	Brasseler USA I Lp	103 packaged and labeled tubes (103 product tubes with 6 pins per tube) of KM168-39-76 Single Diamond Smooth Steinmann Pins were labeled with the incorrect product labels. The tub
2019-11-04	Trilliant Surgical, LLC	The firm has identified that parts from the kit, lot: TSL007202, have the potential to contain the incorrect contents of the 8mm HTR Sterile Hammer Toe Reaming Kit. The kit should
2018-05-16	Zimmer Biomet, Inc.	The firm is recalling various trauma guide wires due to insufficient packaging design verification and exceeding the expected occurrence rate of complaints for sterile barrier fail
2018-05-16	Zimmer Biomet, Inc.	The firm is recalling various trauma guide wires due to insufficient packaging design verification and exceeding the expected occurrence rate of complaints for sterile barrier fail

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.