Arjo Tenor Patient Lift Recall
Certain Arjo Tenor mobile patient lifts may have a defective internal component in the actuator that could suddenly lose its ability to hold the load, causing …
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Every recall we are tracking for ARJOHUNTLEIGH POLSKA Sp. z.o.o., newest first, sourced from the FDA. If you are wondering whether your ARJOHUNTLEIGH POLSKA Sp. z.o.o. 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 ARJOHUNTLEIGH POLSKA Sp. z.o.o. recall posts.
1 recall · updated Mar 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
Boston Scientific is replacing certain FARASTAR Pulsed Field Ablation generators that cannot work with the FARAPOINT catheter. If your generator has an …
Boston Scientific Corporation
The Faradive Steerable Sheath Clear used in cardiac catheterization procedures may allow air to enter the bloodstream if the dilator is inserted incorrectly …
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
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