Health & Personal Care Recalls

Taizhou Kangping Medical 3.85 Million Cartons of BZK Antiseptic Towelettes Recalled for Sterility LQ

Lack of Assurance of Sterility.

AUM Pharmaceuticals Isopropyl Alcohol Prep Pads Recall: 500 Cases Active, High Hazard

51,320 Belsomra Tablets Recalled for Delayed Dissolution Risk — Check Your Lot Numbers

Failed Dissolution Specifications: potential for delayed dissolution of the dose after administration which may result in delayed release of the drug, delaying onset of sleep.

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Recall for Low Dissolution 8,568 Bottles in

Failed Dissolution Specifications: low dissolution results

Summa Therapeutics Recalls 22 Finesse BTK Multicath Angioplasty Balloons Over Burst Specifications (

Potential for the balloon in the device to not meet burst specifications.

DJO Surgical Recalls 447 ALTIVATE Reverse Glenoid Reamer Sleeve Units (2025)

Their is a potential that the reamer may kick or bind up during or immediately prior to use.

DJO Surgical ALTIVATE Reversed Wedge Glenoid Reamer Boss Drill 6.5mm Recalled in 2025 for Binding or

Their is a potential that the reamer may kick or bind up during or immediately prior to use.

DJO Surgical AltiVate Reverse Glenoid Tray Recall Affects 439 Kits Nationwide (2025)

DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.

DJO Surgical ALTIVATE Glenoid Reamer Head Recall Expands to 927 Units

Their is a potential that the reamer may kick or bind up during or immediately prior to use.

6,973 KleenFoam Antimicrobial Foam Soap Cartridges Recalled for Contamination Risk

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

CR Bard Recalls SureStep Foley Tray System A942216 for Incorrect Inserts (2025)

C.R. Bard Recalls 4,300 SureStep Foley Tray System Bardex I.C. Complete Care Catheter Trays (A303316

PeriGiene Health Care Antiseptic Recalled for Burkholderia Contamination (2025)

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

DermaSarra External Analgesic Recalled for Burkholderia Cepecia Contamination (DermaRite Industries)

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

Quest International Measles IgM 01-190M Recall for False Premarket Clearance

Measles IgM Test Kit lacks premarket approval or clearance.

C.R. Bard Recall: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Contains Incorrect Inserts

DermaKleen Antiseptic Lotion Soap Recalled Nationwide for Burkholderia cepacia Contamination (Class

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

Stryker Communications Recalls 40 Medical Light Systems Over Powder Coating Chip Risk (2025)

Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.

BioFire Defense FilmArray NGDS Warrior Panel NGDS-ASY-0007 Recall 130 Kits in 2025

FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead to delayed results and additional diagnostic workup.

Boothwyn Pharmacy Semaglutide 2.5 mg/mL 2 mL Vials Recalled for Subpotent Drug (HIGH)