Orthofix MINIRAIL M101 Recall
Orthofix MINIRAIL external fixation devices were shipped with incorrect model labels. The M101 was labeled as M103, the M103 was labeled as M101, and the M122 …
Orthofix U.S. LLC
Every recall we are tracking for Orthofix U.S. LLC, newest first, sourced from the FDA. If you are wondering whether your Orthofix U.S. LLC product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new Orthofix U.S. LLC recall posts.
1 recall · updated Jun 10, 2026
Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the manifold. This can …
Boston Scientific Corporation
ChloraPrep FREPP sterile skin antiseptic applicators were distributed without proper sterilization, posing a risk of infection. These applicators are used …
CareFusion 213, LLC
Orthofix MINIRAIL external fixation devices were shipped with incorrect model labels. The M101 was labeled as M103, the M103 was labeled as M101, and the M122 …
Orthofix U.S. LLC
ConvaTec is recalling Aquacel Ag Surgical SP surgical dressings (REF 413556, 9cm x 15cm size) because some were made thicker than the design specification. The …
ConvaTec, Inc

SUNS International is recalling SS6291 Solenoid Interlock Switches used in residential elevators because the switch can get stuck in a retracted position, …
SUNS SS6291 Solenoid Interlock Switches
Remel GC Agar Base laboratory media may not properly recover some strains of Neisseria gonorrhoeae bacteria, potentially leading to missed or delayed diagnoses …
Remel, Inc
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