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FDA (Device enforcement)Recalled 2023-09-01class ii

Onkos Surgical, Inc.: Segmental Stem, Canal Filling, Straight, 120MM, 1 EACH. Model Numbers: FS-11120-03M, FS-12120-03M, FS-13120-03M, FS-14120-03M, FS-15120-03M, FS-16120-03M, FS-17120-03M, FS-18120-

Hazard

Potential for breach of Tyvek seals.

Details from the source

Reason for recall: Potential for breach of Tyvek seals. Distribution: Product was shipped from Onkos' distribution in Olive Branch, MS to consignees in the following states: GA, TX, WA, LA, NJ, FL, AZ, MD, MS, KS, IL, WI, KY, PA, NC, NE, OH, HI. Quantity: 120 units Lot/code info: a. Model Number: FS-11120-03M; UDI-DI: B278FS1112003M0; Lot Numbers: 1880532, 1880533, 1880534, 1880535, 1880536, 1880537, 1880538, 1880539, 1880540, 1880541, 1880542, 1880543. b. Model Number: FS-12120-03M; UDI-DI: B278FS1212003M0; Lot Numbers: 1880544, 1880545, 1880546, 1880547, 1880548, 1880549, 1880550, 1880551, 1880552, 1880553. c. Model Number: FS-13120-03M; UDI-DI: B278FS1312003M0; Lot Numbers: 1880554, 1880555, 1880556, 1880557, 1880558, 1880559, 1880560, 1880561, 1880562, 1880563. d. Model Number: FS-14120-03M; UDI-DI: B278FS1412003M0; Lot Numbers: 1880564, 1880565, 1880566, 1880567, 1880568, 1880569, 1880570, 1880571, 1880572, 1880573, 1880574. e. Model Number: FS-15120-03M; UDI-DI: B278FS1512003M0; Lot Numbers: 1880575, 1880576, 1880577, 1880578, 1880579, 1880580, 1880581, 1880582, 1880583, 1880584, 1880585, 1880586, 1880587. f. Model Number: FS-16120-03M; UDI-DI: B278FS1612003M0; Lot Numbers: 1880588, 1880589, 1880590, 1880591, 1880592, 1880593, 1880594, 1880595, 1880596, 1880597, 1880598. g. Model Number: FS-17120-03M; UDI-DI: B278FS1712003M0; Lot Numbers: 1880599, 1880600, 1880601, 1880602, 1880603, 1880604, 1880605, 1880606, 1880607, 1880608, 1880609, 1880610, 1880611. h. Model Number: FS-18120-03M; UDI-DI: B278FS1812003M0; Lot Numbers: 1880612, 1880613, 1880614, 1880615, 1880616, 1880617, 1880618, 1880619, 1880620, 1880621, 1880622, 1880623. i. Model Number: FS-19120-03M; UDI-DI: B278FS1912003M0; Lot Numbers: 1880624, 1880625, 1880626, 1880627, 1880628, 188062

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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