Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,267 results
Food & Beverage
Germany BVLGeneral Alert

Winter Outdoor Schuhe, schwarz

Gesundheitsschädliche Substanz

Jun 24, 2026Wünsche Fashion GmbH & Co.KG, Bei den Mühren 5, 20457 Hamburg
Medical Device
FDA DevicesClass II

Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y ...

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass II

Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ6...

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: 1) BNT CV PACK, Medline Kit Number...

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical ...

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
Medical Device
FDA DevicesClass I

Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3...

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Pharmaceutical
FDA DrugsClass II

Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc (equivalent to 400 units)...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT, Kit Uro Robot Cyst...

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline convenience kits: PORT A CATH DYNJ906818A

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass II

Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All ...

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

Jun 24, 2026GE Medical Systems, LLC
Pharmaceutical
FDA DrugsClass II

Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30...

Defective container:may contain bottles with incomplete seals

Jun 24, 2026Keystone Industries
Medical Device
FDA DevicesClass II

ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Cat...

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
Medical Device
FDA DevicesClass I

Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-00...

Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

Jun 24, 2026Datex-Ohmeda Inc
Pharmaceutical
FDA DrugsClass III

Focalin XR (dexmethylphenidate HCl) 5 mg, 30 extended-release capsules per bottl...

Labeling: Incorrect or Missing Lot and/or Exp Date

Jun 24, 2026Sandoz Inc
Medical Device
FDA DevicesClass II

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: D...

Assayed Whole blood control contains labeling with incorrect performance range.

Jun 24, 2026Accriva Diagnostics, Inc.
Medical Device
FDA DevicesClass I

Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Pharmaceutical
FDA DrugsClass II

VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Act...

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

Jun 24, 2026PAI Holdings LLC
Medical Device
FDA DevicesClass II

Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura ...

Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection

Jun 24, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical Device
FDA DevicesClass II

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING...

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (r...

Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

Jun 24, 2026Datex-Ohmeda Inc
Food & Beverage
UK FSAPublished

Update 1: Traditional Cheese Company recalls French Bries because of contaminati...

The presence of Listeria monocytogenes in the products listed above. Symptoms caused by Listeria monocytogenes can be similar to flu and include high temperature, muscle ache or pain, chills, feeling or being sick and diarrhoea. However, in rare cases, the infection can be more severe, causing serious complications, such as meningitis. Some people are more vulnerable to listeria infections, including those over 65 years of age, pregnant women and their unborn babies, babies less than one month old and people with weakened immune systems.

Jun 24, 2026Traditional Cheese Company
Medical Device
FDA DevicesClass II

Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CV...

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
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