GEM Premier 5000 PAK Cartridge Recall
GEM Premier 5000 PAK cartridges may repeatedly eject during warm-up due to detection errors, requiring cartridge replacement and potentially delaying test …
Instrumentation Laboratory
Instrumentation Laboratory Recalls (2026)
Every recall we are tracking for Instrumentation Laboratory, newest first, sourced from the FDA. If you are wondering whether your Instrumentation Laboratory 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 Instrumentation Laboratory recall posts.
1 recall · updated Jan 20, 2026
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Residential Elevators StrikeLock Door Lock Recall
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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