Class IIOngoingZ-2283-2026
Advanced Bionics, LLC recalls Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mi…
Due to incorrect shelf-life expiration date.
Advanced Bionics, LLCCAJun 10, 2026
Recalls: Under Investigation by firm
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 61–72 of 1,121 recalls
Class IOngoingZ-2278-2026
B Braun Medical Inc recalls Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Descript…
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a rec…
B Braun Medical IncPAJun 10, 2026
Class IOngoingZ-2277-2026
B Braun Medical Inc recalls Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spino…
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a rec…
B Braun Medical IncPAJun 10, 2026
Class IOngoingZ-2276-2026
B Braun Medical Inc recalls Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SP…
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a rec…
B Braun Medical IncPAJun 10, 2026
Class IIOngoingZ-2273-2026
Covidien LLC recalls Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
Temperature probe devices lack FDA clearance.
Covidien LLCCOJun 10, 2026
Class IIOngoingZ-2272-2026
Covidien LLC recalls Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Temperature probe devices lack FDA clearance.
Covidien LLCCOJun 10, 2026
Class IIOngoingZ-2271-2026
Covidien LLC recalls Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
Temperature probe devices lack FDA clearance.
Covidien LLCCOJun 10, 2026
Class IIOngoingZ-2262-2026
Baxter Healthcare Corporation recalls Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number:…
Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slower transfers of ingredients, or system a…
Baxter Healthcare Corp…ILJun 10, 2026
Class IIOngoingZ-2260-2026
Medline Industries, LP recalls Medline medical convenience kit labeled as EYE TRAY-LF
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister pack are labeled as a 1 mL Luer L…
Medline Industries, LPILJun 3, 2026
Class IIOngoingZ-2259-2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura system
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service.…
PHILIPS MEDICAL SYSTEM…Jun 3, 2026
Class IIOngoingZ-2258-2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion system
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service.…
PHILIPS MEDICAL SYSTEM…Jun 3, 2026
Class IIOngoingZ-2241-2026
Medtronic Neuromodulation recalls Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
Medtronic Neuromodulat…MNJun 3, 2026