Activbody, Inc. - Activforce - Class 2 Recall
Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5, the first isometrics-based smart strength training and rehabilitation device. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 17, 2021 Category: Medical Devices Source Type: alerts

Hill-Rom, Inc. - Liko Multirall (a Hill Rom Company) - Class 1 Recall
Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal SlingBar 350 R2R (product number 3156094) Carriage D45 with Double Hook (product number 3136100) Extension belt 300-400 mm (product number 3136226) Extension belt 400-600 mm (product number 3136227) Extension belt 600-1000 mm (product number 3136228) Extension belt 1000-1400mm (product number 3136229) (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2021 Category: Medical Devices Source Type: alerts

Hill-Rom, Inc. - Liko Multirail (a Hill Rom Company) - Class 1 Recall
Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal SlingBar 350 R2R (product number 3156094) Carriage D45 with Double Hook (product number 3136100) Extension belt 300-400 mm (product number 3136226) Extension belt 400-600 mm (product number 3136227) Extension belt 600-1000 mm (product number 3136228) Extension belt 1000-1400mm (product number 3136229) (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2021 Category: Medical Devices Source Type: alerts

MOTEK MEDICAL B.V. - Body Weight Support (BWS) Light - Class 2 Recall
Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mill, Grail, M-Gait - Product Usage: is designed to facilitate functional gait training of subjects with gait and/or balance impairment by providing dynamic partial vertical unloading during walking on a treadmill. The device will be used as an assistive device for gait deficiency rehabilitation and research purposes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 28, 2020 Category: Medical Devices Source Type: alerts

WELCH ALLYN, INC/MORTARA - Class 2 Recall
Q-Tel. The Q-Tel RMS system is a computer-based cardiac and pulmonary rehabilitation data acquisition and editing system. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 30, 2020 Category: Medical Devices Source Type: alerts

ARJOHUNTLEIGH POLSKA Sp. z.o.o. - ArjoHuntleigh Sara Combilizer - Class 2 Recall
ArjoHuntleigh Sara Combilizer; Intended to facilitate early immobilization, rehabilitation, and care of patients. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 12, 2018 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - GENDER SOLUTIONS NATURALKNEE FLEX SYSTEM; NEX GEN COMPLETE KNEE SOLUTION CRFLEX GENDER SOLUTIONS - Class 2 Recall
GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM FEMORAL COMPONENT¿ N-K FLX GSM POR FEM SZ 2 RT N-K FLX GSM POR FEM SZ 3 LT N-K FLX GSM POR FEM SZ 4 LT N-K FLX GSM POR FEM SZ 4 RT N-K FLX GSM POR FEM SZ 5 LT N-K FLX GSM POR FEM SZ 5 RT Components with CSTi porous coating are indicated for uncemented or cemented use in skeletally mature individuals with intact medial and lateral collateral ligaments undergoing primary surgery for rehabilitating knees damaged as a result of Noninflammatory Degenerative Joint Disease (NIDJD) or Inflammatory Joint Disease (IJD). (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 15, 2018 Category: Medical Devices Source Type: alerts

Zimmer Biomet, Inc. - GENDER SOLUTIONS NATURALKNEE FLEX SYSTEM - Class 2 Recall
GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM GENDER SOLUTIONS FEMALE (GSF) FEMORAL COMPONENT NONPOROUS¿ N-K FLX GSF NP FEM SZ 0 RT N-K FLX GSF NP FEM SZ 4 LT N-K FLX GSF NP FEM SZ 4 RT Components with CSTi porous coating are indicated for uncemented or cemented use in skeletally mature individuals with intact medial and lateral collateral ligaments undergoing primary surgery for rehabilitating knees damaged as a result of Noninflammatory Degenerative Joint Disease (NIDJD) or Inflammatory Joint Disease (IJD). (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 15, 2018 Category: Medical Devices Source Type: alerts

Smith & Nephew, Inc. - Modular Necks - Class 2 Recall
Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip components are also indicated for inflammatory degenerative joint disease including rheumatoid arthritis, arthritis secondary to a variety of diseases ...
Source: Medical Device Recalls - January 5, 2017 Category: Medical Equipment Source Type: alerts

Smith & Nephew, Inc. - Modular SMF(TM) - Class 2 Recall
Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip components are also indicated for inflammatory degenerative joint disease including rheumatoid arthritis, arthritis secondary to a variety of diseases...
Source: Medical Device Recalls - January 5, 2017 Category: Medical Equipment Source Type: alerts

Smith & Nephew, Inc. - Modular REDAPT(TM) Hip Systems - Class 2 Recall
Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip components are also indicated for inflammatory degenerative joint disease including rheumatoid arthritis, arthritis secondary to a var...
Source: Medical Device Recalls - January 5, 2017 Category: Medical Equipment Source Type: alerts

Biomet 3i, LLC - LOW PROFILE ABUTMENTS INTERNAL AND EXTERNAL CONNECTION - Class 2 Recall
BIOMET 3i CERTAIN LOW PROFILE 17¿ ABUTMENT 4.1MM(D) X 2MM(H) An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 21, 2016 Category: Medical Equipment Source Type: alerts

Biomet 3i, LLC - LOW PROFILE ABUTMENTS INTERNAL AND EXTERNAL CONNECTION - Class 2 Recall
BIOMET 3i LOW PROFILE ABUTMENT (NON-HEXED) PICK-UP IMPRESSION COPING An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 21, 2016 Category: Medical Equipment Source Type: alerts

Biomet 3i, LLC - LOW PROFILE ABUTMENTS INTERNAL AND EXTERNAL CONNECTION - Class 2 Recall
BIOMET 3i CERTAIN LOW PROFILE ONE-PIECE ABUTMENT 4.1MM(D) X 4MM(H) An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 21, 2016 Category: Medical Equipment Source Type: alerts

Biomet 3i, LLC - LOW PROFILE ABUTMENTS INTERNAL AND EXTERNAL CONNECTION - Class 2 Recall
BIOMET 3i LOW PROFILE ABUTMENT 4.1MM(D) X 1MM(H) An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 21, 2016 Category: Medical Equipment Source Type: alerts