High Risk Recalls

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.

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.

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.

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.

Deale International Recalls CasaClean Handheld Steamers DF-958 Sold on HSN for Burn Risk (2025)

Deale International is recalling CasaClean Handheld Steamers DF-958 sold on HSN for burn risk. The steamers can leak steam or spray boiling water, creating a serious burn hazard. Consumers should stop using the product and contact Deale for a full refund.

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

Primark Recalls DTR Stitch 4-Pack Scented Highlighters for Phthalate Exposure Recall 2025

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.

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

iStore Magnetic Wireless Power Bank Recalled for Fire Hazards in 2025

VIVI Recalls E-Bike 36V Lithium-Ion Batteries Over Fire Hazard (2025)

VIVI recalled 36-volt lithium-ion batteries included with certain VIVI brand e-bikes sold by VIVI. The batteries can overheat and pose fire and burn hazards. Stop using affected e-bikes immediately and contact VIVI for a free replacement battery and charger.

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.

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

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

Measles IgM Test Kit lacks premarket approval or clearance.

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.

AUGNORYE Padded Crib Bumpers Recalled for Suffocation Risk Sold on Amazon by YIXIA (2025 Recall)

AUGNORYE recalled padded cushioned crib bumpers sold on Amazon by YIXIA. The bumpers can obstruct an infant's breathing, creating a suffocation hazard. Parents should stop using immediately and contact YIXIA for a full refund.

Dearlomum Retractable Safety Gate Recall 2025 for Entrapment Hazard (SH20.006D)

SPPTTY Kids Bicycles Recalled for Lead Poisoning Risk (2025)

This recall involves SPPTTY kids bicycles. The bicycles are pink with brown seat covers, brown handlebars, brown pedals and brown baskets and were sold in 14-inch and 18-inch sizes. The brand "SPPTTY" and "New Sport Bike" are printed on the downtube.