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Last updated: 2024
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Recall class: Type II
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Displaying 61 - 75 of 232 items.
Sanis Health Duloxetine 60 mg Capsule; Exceeds acceptable interim intake limit for N-nitroso-duloxetine (NDLX)
RecallHealth product recall | 2024-05-16
Sandoz Fesoterodine Fumarate 8 mg tablet; Out-of-specification (diester impurity)
RecallHealth product recall | 2024-05-16
Philips Hemodynamic Application
RecallHealth product recall | 2024-05-16
Synchro Guidewires
RecallHealth product recall | 2024-05-15
Luer Slip and Luer Lock Syringes
RecallHealth product recall | 2024-05-09
MED-RX® Epidural Anesthesia Kit
RecallHealth product recall | 2024-05-09
HistoCore Arcadia H
RecallHealth product recall | 2024-05-08
Alcon Ophthalmic Knife
RecallHealth product recall | 2024-05-08
Stryker ProCuity Beds
RecallHealth product recall | 2024-05-08
Integra Cranial Kit
RecallHealth product recall | 2024-05-08
Vyaire Medical Twin Tube Probenschlauch
RecallHealth product recall | 2024-05-08
Presource® Kits Containing Curity® Flexible Adhesive Bandage X-large Components
RecallHealth product recall | 2024-05-07
IOMAX Cortical Module
RecallHealth product recall | 2024-05-07
MyoSPECT Molecular Imaging
RecallHealth product recall | 2024-05-07
Fresenius Blood Pump Rotor
RecallHealth product recall | 2024-05-06