XTANT MEDICAL Xpress Pedicle Screw Recall
XTANT MEDICAL Xpress Pedicle Screw System units (Part Number X073-6555-DL, 6.5 x 50 mm) from one lot were mislabeled with an incorrect part number, making the …
XTANT Medical Holdings, Inc
XTANT Medical Holdings, Inc Recalls (2026)
Every recall we are tracking for XTANT Medical Holdings, Inc, newest first, sourced from the FDA. If you are wondering whether your XTANT Medical Holdings, Inc 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 XTANT Medical Holdings, Inc recall posts.
1 recall · updated Feb 18, 2026
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SUNS International is recalling SS6291 Solenoid Interlock Switches used in residential elevators because the switch can get stuck in a retracted position, …
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Residential Elevators is recalling its StrikeLock hoistway door locking device, used on residential elevator landing doors. The defective lock can allow the …
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BD PurPrep Povidone-Iodine Recall
BD PurPrep povidone-iodine sterile skin prep solution (25 applicators per carton) may not be sterile due to potential product contamination. Using a non-sterile …
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BD PurPrep Povidone-Iodine Recall
BD PurPrep povidone-iodine sterile solution applicators (10.5 mL, 25-pack) are being recalled because the manufacturer cannot confirm they are properly …
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Philips SmartPath dStream MRE Recall
Philips SmartPath to dStream 3.0T MR Elastography systems can produce incorrect stiffness measurements when certain image settings are used together. This may …
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Physio-Control LIFEPAK Defibrillator Recall 2026
Physio-Control is recalling certain LIFEPAK defibrillators that were serviced between July 2023 and November 2025 without confirmed completion of a required …
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