battery powered Recalls

Philips Allura Xper FD10 OR Table 722033 Recall 2 Units Worldwide (2025)

Philips Medical Systems Nederland Faces High-Risk Recall for Allura Xper FD20/15 BIOS Battery

Philips Allura Xper FD10 Recalled for BIOS Battery Startup Failure (2,317 Units Worldwide, 2025)

Philips Allura Xper FD10C Recall for 2 US Units Over BIOS Battery Startup Failure (2025)

Philips Recalling 298 Allura Xper FD20 OR Tables Worldwide Over BIOS Battery Risk (2025)

LeMaitre Vascular Artegraft Collagen Vascular Grafts Recall 2025: 28 U.S. Units Affected

The bovine carotid arteries used to produce the impacted grafts from affected lots were sourced using raw material from a supplier that had not been reviewed and approved by the appropriate regulatory authority.

BigTree Sales Recalls BT-GERMWAND-LRG-WHT UV-C Wand for Unsafe Radiation Risk (2025)

Northeast Scientific NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter Recall 2026

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

Northeast Scientific NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter Recall 173 Un­

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter Recall: 616 Units In US Distribution

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

Getinge 88-Series Washer-Disinfector 88-5 Recalled for Overheat Risk in 788 Units (2025)

Potential for device to overheat during operation f the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.

Party Favors Lite-Up Torches and Laser Pointers Recalled for Battery Ingestion Risk

Party Favors recalled four models of lite-up torches and laser pointers due to risk of serious injury or death from swallowed button cell batteries. Imported by MTC Trading. Consumers should stop using the products and seek a full refund.

Lulive 12-Drawer Dressers Recalled for Tip-Over Risk in 2025

CT-ENERGY Recalls nc-02 Lithium Coin Battery Chargers Over Battery Ingestion Risk (2025)

Granules Pharmaceuticals Amphetamine Capsules Recalled for Impurities Degradation Standards (2025)

Siemens MAGNETOM Vida MRI Recall 237 Units Worldwide Over Ice Blockage Risk (2025)

Siemens MAGNETOM Verio Dot MRI Recall 30 Units Over Ice Blockage Risk (2025)

B. Braun Sterile Water for Injection 3000 mL Recall Affects 26,316 Bags Over Sterility Concerns (202

Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment.

Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected

Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.

GE Medical Systems MAC VU360 Recall 29,225 Trunk Cable and Module Holder Units (2025)