45 results
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49ms
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Sources: EU EUDAMED, US FDA
Health-Mor, Inc
FDA registration
Health-Mor, Inc·1 product·🇺🇸 United States
PUMP MMT-1714K 630G BLACK MMOL CANADA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 17, 2019
COR HEALTH, INC
FDA registration
COR HEALTH, INC·2 products·🇺🇸 United States
COULTER AC*T 5 DIFF ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·May 12, 2011
INTELLIFILL I.V. DEVICE
FDA Adverse Event
Other
·FOR HEALTH TECHNOLOGIES, INC.·Product code NEP·July 8, 2009
COATED VICRYL
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 3, 2026
SUREFORM
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC·Product code GDW·June 8, 2022
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, right, 19 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-021-19. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 11 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-11. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 9 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-09. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 13 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-13. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, right, 16 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-021-16. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1 or 2, right, 9 MM height, for use with baseplate size 1, 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-021-09. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, left, 13 MM height, for use with baseplate size 1 or 2 sterile, Zimmer, Warsaw, IN; REF 00-5424-011-13. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, right, 16 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-021-16. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, left, 11 MM height, use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-011-11. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, right, 19 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-021-19. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 19 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-19. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, left, 9 MM height, use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-011-09. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, right, 11 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-021-11. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.
FDA Recall
Terminated
·Zimmer Inc.·Product code JWH·October 8, 2009