Search U.S. Product Recalls Database

Showing 4321–4340 of 22584 results

Sort:

Newest first Oldest first

Leg Bag (Medline) – undeclared latex (2023)

Undeclared Allergen

Undeclared latex

Moderate

FDAOct 19, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Para-Pak Zn-PVA (Meridian) – leakage risk (2023)

Plastic vials contain a manufacturing defect may cause an increased risk of leakage and presents a risk of incidental exposure to biological hazards associated with direct contact with the patient specimen.

High

FDAOct 19, 2023Nationwide• Meridian Bioscience Inc

Stay Informed

Search Product Recalls

Leg Bag (Medline) – undeclared latex (2023)

Para-Pak Zn-PVA (Meridian) – leakage risk (2023)

ARCHITECT c4000 Processing Module (Abbott) – undeclared latex (2023)

Combo Kit (Integra) – packaging defect (2023)

Cranial Access Kit (Integra) – packaging defect (2023)

Modular Cooler-Heater (CardioQuip) – heater malfunction (2023)

Cranial Access Kit (Integra) – packaging defect (2023)

Cardinal Health Stool Kit (Meridian) – leakage risk (2023)

Leg Bag (Medline) – undeclared latex (2023)

Alinity c Processing Module (Abbott) – undeclared latex (2023)

Para-Pak Clean Vial (Meridian) – leakage risk (2023)

Leg Bag (Medline) – undeclared latex (2023)

Alinity i Processing Module (Abbott) – undeclared latex (2023)

KWIKSTIK P. venetum (Microbiologics) – contamination risk (2023)

Monarch Platform (Auris Health) – image view risk (2023)

LYFO-DISK P. venetum (Microbiologics) – contamination risk (2023)

Lugol's Iodine Solution (EMD Millipore) – packaging seal issue (2023)

ARTIS icono (Siemens) – collision sensor problem (2023)

FilmArray TORCH (BioFire) – power switch risk (2023)

SagiPlan 2.2 (Bebig) – measurement accuracy issue (2023)