Eugia US LLC recalls 168,300 vials of Lidocaine HCl Injection nationwide due to barcode obscuration on label wrap, classified as Class III with no expected health risk.
B. Braun Medical Class II recall of CESK Harris Methodist adhesive product (690 units nationwide) due to potential butyrate tubing cracking that renders product unusable.
BD Spinal Tray with Whitacre Needle product recall (Class I) affects 330 units nationwide due to bupivacaine quality deficiencies identified during FDA inspection.
B. Braun Medical recalls 16,080 Spinocan spinal needle procedure kits nationwide due to potential quality issues with Bupivacaine Hydrochloride in Dextrose Injection identified during FDA inspection.
Dräger's Atlan A350XL anesthesia workstation (Model 8621600) is subject to a Class I recall affecting 394 units distributed across the US and internationally due to piston ventilator failure risks during use.
CareFusion's BD Pyxis MedBank Tower medication cabinet (607 units nationwide and internationally) is subject to a Class II recall due to fingerprint scanner overheating risk causing first-degree burns.
Kico Knee Innovation Company issues Class II recall of Arvis Hip & Knee 3.0 instrument components (69 units nationwide and internationally) due to potential magnet corrosion that may cause temporary health complications.
Kayserbetten GmbH & Co. KG issues Class I recall of KayserBett IDA pediatric care beds due to risk of entrapment or death if hand control adjustment functions are not locked when children are unattended.
Daavlin Distributing Company recalls 368 units of Phothera 200 phototherapy devices nationwide due to reversed calibration outputs that may cause temporary health effects; Class II recall.
GE Medical Systems recalls 16 Class II electrocardiograph systems worldwide due to software that may associate clinical information with incorrect patients, affecting units in Florida, Georgia, India, Italy, South Korea, and the United Kingdom.
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