-
STRYKER PKG., SINGLE SPIKE TUBE SET recall
FDA
· Stryker Corporation · Class II
-
STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING recall
FDA
· Stryker Corporation · Class II
-
STRYKER AHTO TUBE SET WITH TIP PACKAGING recall
FDA
· Stryker Corporation · Class II
-
STRYKER AHTO TUBE SET PACKAGING recall
FDA
· Stryker Corporation · Class II
-
DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model recall
FDA
· Nuclein LLC · Class II
-
Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40… recall
FDA
· Maquet Critical Care AB · Class II
-
Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System recall
FDA
· Innovasis, Inc · Class II
-
Medical Action Industries Product Name: Dialysis Change Tray Clear… recall
FDA
· Medical Action Industries, Inc. 306 · Class II
-
OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model recall
FDA
· Oxos Medical Inc · Class II
-
munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control… recall
FDA
· Munevo Gmbh · Class II
-
Nerivio Infinity recall
FDA
· Theranica Bioelectronics Ltd · Class II
-
WASPLab Product Name: WASPLab Model recall
FDA
· Copan WASP · Class II
-
Quantum Rehab Product Name: Quantum Rival Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: 4Front Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Quantum 4Front 2HD Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Q6 Edge 4 Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Q6 Edge 3 Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Q6 Edge 2.0 (ilevel) Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Quantum 1450 Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum rehab Product Name: Q6 Edge 2.0 Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Q6 Edge HD Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: R-TRAK Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Q6 Edge 3 Stretto Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Quantum Outback Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Quantum Rehab Product Name: Quantum 4Front 2 Model recall
FDA
· Pride Mobility Products Corp. · Class II
-
Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN:… recall
FDA
· Boston Scientific Corporation · Class II
-
Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions… recall
FDA
· Boston Scientific Corporation · Class II
-
Radial Jaw 4 Standard Capacity Biopsy Forceps with the following… recall
FDA
· Boston Scientific Corporation · Class II
-
Kingfisher Compact Individual First Aid Kit recall
FDA
· Integrated Medcraft LLC · Class II
-
FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12) recall
FDA
· Integrated Medcraft LLC · Class II
-
Charger for the Therabody Theragun, G4 PRO massage device… recall
FDA
· Therabody, Inc · Class II
-
REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The… recall
FDA
· Beckman Coulter Biomedical GmbH · Class II
-
Stryker Hoffmann II Connecting Rod Micro 3 x 150mm recall
FDA
· Stryker GmbH · Class II
-
Stryker Hoffmann II Connecting Rod Micro 3 x 120mm recall
FDA
· Stryker GmbH · Class II
-
Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall
FDA
· Stryker GmbH · Class II
-
Stryker Hoffmann II Connecting Rod Micro 3 x 60mm recall
FDA
· Stryker GmbH · Class II
-
Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall
FDA
· Stryker GmbH · Class II
-
Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall
FDA
· Stryker GmbH · Class II
-
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall
FDA
· Stryker GmbH · Class II
-
GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
FDA
· Instrumentation Laboratory · Class II
-
GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
FDA
· Instrumentation Laboratory · Class II
-
GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
FDA
· Instrumentation Laboratory · Class II
-
GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
FDA
· Instrumentation Laboratory · Class II
-
GEM Premier 7000 with iQM3 Product Name: GEM Premier 7000 with iQM3 Model recall
FDA
· Instrumentation Laboratory · Class II
-
GEM Premier 5000 with IQM2 Model recall
FDA
· Instrumentation Laboratory · Class II
-
OsteoBallast, 45 x 17.5 mm (SeaSpine Brand) recall
FDA
· IsoTis OrthoBiologics, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Loop… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Block… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Heart… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1)… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL… recall
FDA
· Windstone Medical Packaging, Inc. · Class II
-
EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary… recall
FDA
· Medtronic Perfusion Systems · Class II
-
EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with… recall
FDA
· Medtronic Perfusion Systems · Class II
-
EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR… recall
FDA
· Medtronic Perfusion Systems · Class II
-
EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR… recall
FDA
· Medtronic Perfusion Systems · Class II
-
EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR… recall
FDA
· Medtronic Perfusion Systems · Class II
-
EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR… recall
FDA
· Medtronic Perfusion Systems · Class II