Synthes Produktions GmbH - MatrixMIDFACE Screws - Class 2 Recall
MatrixMIDFACE Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial skeleton in procedures such as craniotomies, reconstructive procedures, fracture repair, osteotomies, and selective orthognathic surgery of the maxilla and chin. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 31, 2020 Category: Medical Devices Source Type: alerts

Synthes, Inc. - MatrixNEURO Screws - Class 2 Recall
MatrixNEURO Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial skeleton in procedures such as craniotomies, reconstructive procedures, fracture repair, osteotomies, and selective orthognathic surgery of the maxilla and chin. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 25, 2020 Category: Medical Devices Source Type: alerts

Skeletal Kinetics, Llc - CranioSculpt C, 10cc, Bone Void Filler - Class 2 Recall
Cranio/Sculpt C, 10cc, Bone Void Filler, UDI: 00813845021129 - Product Usage: CRANIO/SCULPT C is a calcium phosphate bone void filler indicated for the repair or filling of neurosurgical burr holes, other cranial bone defects and craniotomy cuts with a surface area no larger than 25cm2. CRANIO/SCULPT C may be used in the restoration or augmentation of bony contours of the cranial bone skeleton. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 21, 2020 Category: Medical Devices Source Type: alerts

Medline Industries Inc - Medline convenience kits containing - Class 2 Recall
Custom convenience kits containing Medline brand Sterile Pre-Saturated Povidone Iodine Sponge Products, labeled as follows: Part Description Part Number ABDOMINAL HYSTERECTOMY DYNJ906478 ABDOMINAL HYSTERECTOMY DYNJ906478A ACCESSORY HIP PACK-LF DYNJ0781865M ARTHRO/SHOULDER PACK DYNJ30056J ARTHRO/SHOULDER PACK DYNJ30056K ARTHRO/SHOULDER PACK DYNJ30056L ARTHRO/SHOULDER PACK DYNJ30056M BODY PACK DYNJ55107A BODY PACK DYNJ55107C BODY PACK DYNJ55107D C SECTION CDS CDS984613D C SECTION CDS CDS830172I C SECTION CDS CDS984613F C SECTION CDS CDS830172J C SECTION PACK CMPJ17294I C SECTION PACK-LF DYNJ64834 CARDIAC A & B SJ PACK DY...
Source: Medical Device Recalls - May 16, 2020 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - Biomet Microfixation RapidFlap - Class 2 Recall
Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1040-12 Used for the re-attachment of the bone flap after a craniotomy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 7, 2018 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - Biomet Microfixation RapidFlap - Class 2 Recall
Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Ref Number: 75-1040 Used for the re-attachment of the bone flap after a craniotomy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 7, 2018 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - Biomet Microfixation RapidFlap - Class 2 Recall
Biomet Microfixation RapidFlap System, 12MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1020-12 Used for the re-attachment of the bone flap after a craniotomy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 7, 2018 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - Biomet Microfixation RapidFlap - Class 2 Recall
Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1030-12 Used for the re-attachment of the bone flap after a craniotomy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 7, 2018 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - Biomet Microfixation RapidFlap - Class 2 Recall
Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Ref Number: 75-1030 Used for the re-attachment of the bone flap after a craniotomy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 7, 2018 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - Biomet Microfixation RapidFlap System - Class 2 Recall
Biomet Microfixation RapidFlap System 12mm SpinDown Clamp, sterile Ref Number: 75-1020 Used for the re-attachment of the bone flap after a craniotomy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 7, 2018 Category: Medical Devices Source Type: alerts

Pro-Med Instruments Gmbh - DORO LUCENT Base Unit - Class 1 Recall
DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 18, 2018 Category: Medical Devices Source Type: alerts

Pro-Med Instruments Gmbh - DORO LUCENT Locking Transitional Member - Class 1 Recall
DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 18, 2018 Category: Medical Devices Source Type: alerts

Pro-Med Instruments Gmbh - DORO LUCENT Transitional Member - Class 1 Recall
DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 18, 2018 Category: Medical Devices Source Type: alerts

Stryker Leibinger GmbH & Co. KG - QuickFlap - Class 2 Recall
QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01521S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures in adults and adolescents (age 12 and higher). (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 30, 2018 Category: Medical Devices Source Type: alerts

Stryker Leibinger GmbH & Co. KG - QuickFlap - Class 2 Recall
QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01520S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures in adults and adolescents (age 12 and higher). (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 30, 2018 Category: Medical Devices Source Type: alerts