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.
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls PERIARTICULAR PLATES SHOULDER, PERI PROX LAT HUMERAL, Item Nos. 00234800104 00234800106 00234800108 00234800110 0023
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Universal Locking Plates Sterile, Item Nos. 47492800207 47492800303 47492800402 47492800403 47492800407 474928005
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 47235802106 4723580210
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls DIST LAT FEM LCK PLATE STERILE, Item Nos. 47235710106 47235710110 47235710114 47235710118 47235710122 47235710210
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 47235700310 47235700312 472
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 00
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Periarticular Plates - Tibial, Item Nos. 00234700304 00234700306 00234700308 00234700310 00234700312 00234700314 0
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls TM Ankle and Ankle Talus L/R, Item Nos. 00450001100 00450001200 00450001300 00450001400 00450001500 00450001600 00
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls ZPLP Fibular Plate, Item Nos. 00234701504 00234701506 00234701508 00234701510 00234701512 00234701516 00234701604
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls NCB PERIPROSTHETIC, "NCB PP PROX FEM PLATE", Various sizes, Item Nos. 0202263009 0202263012 0202263015 0202263018 02
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls NCB Proximal Lateral Tibia, "NCB-PT LAX PROX 3H TIBIA", Various Sizes, Item Nos. 0202261205 0202261207 0202261209 020
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Various Custom Devices, Item Nos. 32855090246 32855090252 32855090256 32855090265 32855090266 32855090270 32855090
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Coorad Morrey Total Elbow, Item Nos. 32810502501 32810502701 32810502900 32810503000 32810600012 32810600013 32855
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Sidus Stem-Free Shoulder Humeral Head, Item Nos. 0104555380 0104555400 0104555420 0104555440 0104555460 0104555480
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Trabecular Metal Reverse Shoulder System, Item Nos. 00434210613 00430900103 00434210613 00434210813 00434210817 004
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
November 13, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls BF Humeral Stem, Various Sizes, Item Nos. 00430000606 00430000613 00430000706 00430000713 00430000813 00430000817
Hazard: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 87 mm Item # 195254
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 83 mm Item # 195253
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 79 mm Item # 195252
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 75 mm Item # 195251
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 73 mm Item # 195250
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 71 mm Item # 195249
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 69 mm Item # 195248
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 67 mm Item # 195247
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 65 mm Item # 195246
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 63 mm Item # 195245
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 59 mm Item # 195750
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 63 mm Item # 195751
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 65 mm Item # 195752
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 67 mm Item # 195753
Hazard: The locking bar not fully engaging