Zimmer Biomet Recalls
875 recalls on record · January 20, 2016 to December 30, 2020 · Medical Devices
Recalls by year
16
17
18
19
20
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 4, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls HENNESSY LEFT CONST GLENOID HA, Item No. PM555360 UDI (01)00880304819597(17)260425(10)664030 Product Usage: Constrai
Hazard: Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
December 4, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Usage: Arcomium replacement.
Hazard: Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
December 4, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls COMP RVRS Shoulder Baseplates, including Custom Products, Item numbers 115331S 115331 115330S 115330 110040610 1100
Hazard: Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
December 4, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Compress, Mini Compress; Item Nos. 178350 178351 178352 178353 178354 178355 178356 178357 178358 178359 17836
Hazard: Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
December 4, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Hazard: The potential that the end of the shaft could fail to effectively mate with the broach with the Calcar Planar Shaft instrument, part number 110032331.
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls cable button for NCB¿ Polyaxial Locking Plate, 2.5 mm Hex Drive, Item No. 47223206001
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Cephalomedullary Nail (CMN), Various sizes, Item Nos. 47249318009 47249318010 47249318011 47249318013 47249318014 4
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Ceramic Femoral Heads, various sizes, Item Nos. 00877504001 00877504002 00877504003 00877504004
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Metasul Femoral Heads, various sizes, Item Nos. 00877004001 00877004002 00877004003 00877004004 00877004005
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Metasul Taper Liner, various sizes, Item Nos. 00877000528 00877000628 00877000732 00877000832 00877000936 008770010
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls FEMOROTIBIAL/FEMORAL NAIL, various sizes. Item Nos. 32855331111 32855331113 32855331115 32855331161 32855331163 328
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls NCB-PH Plate with 4/5/7 Lock Holes, Item Nos. 0202262104 0202262105 0202262107
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls NCB Straight Narrow Plate, various sizes, Item Nos. 0202267008 0202267010 0202267012 0202267014 0202267016 02022670
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Connection Screw for NCB Plate, Item No. 0202266002
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various temporary devices used during the implantation of the device system: bone fixation plates and screws, drill bits
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various fixation systems and accessories, Item Nos. 00224000916 00224000918 00224000920 00224000922 00224000924 002
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various fixation systems and accessories, Item Nos. 00118100522 00118100527 00118100530 00118100532 00118100535 001
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various Knee Systems, Item Nos. 32855411838 32855411840 32855411842 32855411843 32855420307 32855420308 3285542030
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls LPS-MOB ART SURF IMPL D 9MM
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various Devices for Limb salvage arthroplasty, Item Nos. 00585000011 00585001201 00585001202 00585001301 00585001302
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various Surgical Instruments: Screws and Reamers, Item Nos. 00579104100 00579104200 00579104300 00579104400 00579105
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos. 00522000100 00522000200 00522000300 0052
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Fitmore Hip Stem, hip prosthesis, various sizes, Item Nos. 0100551102 0100551103 0100551104 0100551105 0100551106 0
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls CLS Brevius Stem Kinectiv, hip prosthesis, various sizes. Item Nos. 0100296050 0100296060 0100296070 0100296080 0100
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 00151505040 001515
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 47235800515 47235800519 4
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls PROX LAT HUMERAL LOCK PLATE, Item Nos. 47235800104 47235800106 47235800108 47235800112 47235800116 47235800204 472
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos. 00234801303 00234801304 00234801306 00234801308 0023480131
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Periarticulare Plates - Elbow, Humeral and Ulna Plates, Item Nos. 00234800504 00234800506 00234800508 00234800510 00
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).