suffocation risk Recalls

B Braun Medical Recall Expands for Epidural Tray and Catheter Over Lid Positioning Issue (2025)

Potential for the lid of the catheter connector to be in the incorrect position.

Percussionaire IPV In-Line Valve Recall Aims to Stop Use Over Leakage Risk in Ventilators

Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)

InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.

FUJIFILM Healthcare CH-200 Recalled for Broken X-ray Tube Shaft in 16 Units

It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was broken while being operated toward the front while lifting.

Private Label Skin Care Benzoyl Peroxide 10% Recall for Benzene Contamination

Private Label Skin Care recalls Artisan of Skin Benzoyl Peroxide 10% cream after benzene detected. The product was distributed in California and Georgia. Consumers should stop use immediately and contact the company for guidance.

Private Label Skin Care Inc. Benzoyl Peroxide Cleanser Recalled for Benzene Contamination (2025)

Private Label Skin Care Inc. recalled edunn clarity BP Treatment Cleanser 10% after benzene was detected. The recall covers lot numbers 58170A and 58172A with expiration September 2025. The product was distributed in California and Georgia.

Skin MD Body Acne Cleanser Recalled for Elevated Benzene Levels (2025)

Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.

GE Medical Systems Israel Recalls 11 Elscint Cardial Gamma Cameras in 2025

Shanghai United Imaging Healthcare CT X-ray System uCT 550 MD Recall for 22 Units in 2025

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

UIH Technologies PET/CT System Recall Affects 3 Units Over Gantry Interference Risk (2025)

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

Epoca International Recalling Paris Hilton Mini Beauty Fridges Over Fire and Burn Hazard

Medline Excelsior Medical 0.9% Saline Flush Syringes Recalled Over Concentration Deviation (8.27M)

Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.

Olympus BF-H190 Bronchovideoscope Recall Expanded for IFU Updates in 2025

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus BF-1TQ170 Bronchoscope Recall Expanded for IFU Clarifications

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Harris Teeter recalls Asiago Texas Toast for undeclared milk in 295 units

Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefore the allergen milk was not listed in the contain statement.

Olympus BF-1T60 Bronchofiberscope Recall for IFU Updates (2025)

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus BF-1TH1100 Bronchoscope Recall Expanded for IFU Clarifications (2025)—High Risk

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus BF-XT190 Bronchovideoscope Recall for IFU Updates Over Laser and HF Therapy Use

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus BF-PE2 Bronchoscope Recall Expands with 4,289 Units Aboard Outside US

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

CareFusion 303 BD Alaris Infusion Sets Recalled for Flow, Bolus Accuracy Issues (2025)

Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.