13 results · 27ms · Sources: EU EUDAMED, US FDA

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Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product reference : A06010130

FDA Recall
Open, Classified ·Product code KWP·September 16, 2019

Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140

FDA Recall
Open, Classified ·Product code KWP·September 16, 2019

IMPIX DLIF, REF numbers: a) B16123509, b) B16123511, c) B16124009, d) B16124013, e) B16124509, f) B16124511, g) B16124513, h) B16164009, i) B16164013, j) B16165009, k) B16165013; intervertebral fusion device - lumbar

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code MAX·July 12, 2023

IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B20171953, g) B20171963, h) B20171973, i) B20172253, j) B20172263, k) B20172273; intervertebral fusion device - cervical

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code ODP·July 12, 2023

GRANVIA-C, REF numbers: a) A13111427, b) A13112567, c) A13113456, d) A13131516, e) A13131789, f) A13132012, g) B13111014, h) B13111015, i) B13111016, j) B13111017, k) B13111025, l) B13111026, m) B13111027, n) B13111034, o) B13111035, p) B13111036; intervertebral fusion device - cervical

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code MJO·July 12, 2023

IMPIX C+, REF numbers: a) B20240104, b) B20240105, c) B20240106, d) B20240107, e) B20240205, f) B20240206, g) B20240207, h) B20240208; intervertebral fusion device - cervical

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code ODP·July 12, 2023

IMPIX ALIF, REF numbers: a) B15111209, b) B15111212, c) B15111409, d) B15111412; intervertebral fusion device - lumbar

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code MAX·July 12, 2023

IMPIX S, REF numbers: a) B15328071S, b) B15328073S, c) B15328074S, d) B15334072S, e) B15334073S, f) B15334074S; intervertebral fusion device - cervical

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code MAX·July 12, 2023

IMPIX TLIF, REF numbers: a) B15130607S, b) B15130609S, c) B15130611S, d) B15130613S, e) B15130615S, f) B15900806, g) B15900906, h) B15901006, i) B15901106, j) B15901206, k) B15901306; intervertebral fusion device - lumbar

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code MAX·July 12, 2023

IMPIX 3D, REF numbers: a) B242C09122810, b) B242C10062810, c) B242C10122810, d) B242C11062810, e) B242C11122810, f) B242C12062810, g) B242C12122810, h) B242C12123310, i) B242C13062810, j) B242C13122810, k) B242C14122810, l) B242C15122810, m) B247C07062410, n) B247C07062810, o) B247C07063210, p) B247C08062410, q) B247C08062810, r) B247C08063210, s) B247C09062410, t) B247C09062810, u) B247C09063210, v) B247C10062410, w) B247C10062810, x) B247C10063210, y) B247C11062410, z) B247C11062810, aa) B247C11063210, bb) B247C12062410, cc) B247C12062810, dd) B247C12063210, ee) B247C13062410, ff) B247C13062810, gg) B247C13063210, hh) B247C14062410, ii) B247C14062810, jj) B247C14063210, kk) B247C15062810, ll) B247C15063210; intervertebral fusion device - lumbar

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code MAX·July 12, 2023

IMPIX MANTA, REF numbers: a) A20150407, b) A20250407, c) A20350567, d) B20181743, e) B20181753, f) B20181763, g) B20181773, h) B20181943, i) B20181953, j) B20181963, k) B20181973, l) B20182253, m) B20182263; intervertebral fusion device - lumbar

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code ODP·July 12, 2023

IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code OVD·July 12, 2023

PASS LP, REF numbers: a) B02315535Z, b) B02315540Z, c) B02315545Z, d) B02315550Z, e) B02316535Z, f) B02316540Z, g) B02316545Z, h) B02316550Z, i) B02317540Z, j) B02317545Z, k) B02317550Z; intervertebral fusion device - cervical

FDA Recall
Open, Classified ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code MNI·July 12, 2023