Second Nature Brand recalls 24,756 units of Keto Crunch Smart Mix nationwide due to undeclared allergens (cashews, pistachios) and dried cherries that may cause temporary health problems.
Terra Medi LLC recalls 300 units of Hellas Meze Golden Smoked Whole Herring across MA, NJ, IL, and NY due to botulism contamination risk in un-eviscerated fish.
Creative Compounds LLC recalls 2055kg of Betaine Anhydrous 98% distributed to five states due to possible carbon steel foreign material contamination posing temporary health risks.
Fresenius Kabi USA recalls 32 Ivenix Infusion System units nationwide due to a Class I software defect that may cause false battery warnings and unintended pump shutdowns.
Grace Medical Class II recall of 7 stapes prosthesis devices nationwide due to incorrect functional length labeling that may cause temporary or reversible health problems.
Stryker Corporation recalls one Neptune Smart Docking Station (catalog 0770-100-000, SN 2521008873) distributed in Indiana due to unverifiable safety testing and potential electrical shock risk.
Covidien LLC recalls 128,900 Mon-a-Therm temperature probe units nationwide due to lack of FDA clearance, posing risk of temporary or reversible health problems.
Philips recalls 27 Azurion 3M15 X-ray systems nationwide due to Class II defect causing dark, non-diagnostic images during fluoroscopy after pedal tap activation.
Bayer Medical Care recalls Avanta Multi-Patient Administration Tube Sets (catalog AVA 500 MPAT Part 2) due to fit issues with the Contrast Flow Control Valve interface that may cause stopcock disengagement during contrast injection procedures.
Spectra Medical Devices recalls 210,625 units of Lidocaine HCl Injection USP nationwide due to sterility assurance deficiency, classified as Class II risk for temporary health effects.
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