Federal regulations

Super World Trading Inc. recalls 595 cases of tangerine-flavored roasted peanuts distributed across 18 states due to banned cyclamate sweetener content.

GE Healthcare SIGNA Premier whole-body MR scanners subject to Class II recall affecting 41 units due to ferrous fittings that may cause personnel injury during service procedures near active magnets.

Intuitive Surgical da Vinci S and Si Permanent Cautery Hook instruments (Model 420183) are subject to a Class II recall affecting 6,152 units nationwide and internationally due to frayed or broken pitch cables on reusable surgical instruments.

Burlington Medical recalls 5,198 units of wrap aprons and related Class II products worldwide due to potential attenuation degradation that may shorten product lifespan.

Amneal Pharmaceuticals recalls 784 cartons of mislabeled Magnesium Sulfate IV bags nationwide that contain Tranexamic Acid instead, posing serious health risks.

K.C. Pharmaceuticals artificial tears eye drops (589,848 bottles nationwide) are subject to a Class II recall due to lack of sterility assurance, which may cause temporary or reversible health problems.

Intuitive Surgical recalls 7,819 da Vinci S and Si Mega Needle Driver instruments worldwide due to broken or frayed grip cables that may cause temporary health problems.

Synthes USA Products recalls 77 units of 2.4 Volt Tap Locking Screw Tap (Class II) due to lot swap resulting in incorrect threading; distributed nationwide across 22 states.

BD Kiestra ReadA lab automation system (Catalog No. 446948) issued Class II recall affecting 82 units for potential connectivity issues causing delays in plate retrieval after system reboot, with no impact on test results or sample integrity.

Cardinal Health recalls 198,900 tuberculin syringes (catalog 1180100777) distributed nationwide and in Canada due to mislabeled packaging containing U-100 insulin syringes instead.

Siemens Healthcare Diagnostics Class II recall of Atellica CH Enzymatic Hemoglobin A1c test (SMN 11097536) due to potential depressed results when processing with RCRP on the same analyzer.

Pocas International Corp. recalls 148 cases of popping boba ready-to-drink beverages distributed across nine US states and Canada due to packaging integrity issues that may compromise product quality.

Philips Medical Systems recalls 3,552 Vue Motion V12 ultrasound systems (Product 1017979) worldwide due to potential frame sequencing errors during dynamic imaging that may cause temporary health complications.

Abiomed recalls 33,107 Generation 1 purge cassettes distributed worldwide in Impella Pump Sets due to increased purge leak risk that may cause serious injury or death.

ReCor Medical's Paradise ultrasound renal denervation catheter (Model PRDS-068-02) is subject to a Class II recall affecting 24 units distributed across nine U.S. states due to nonconforming product that should have been scrapped.