MonojectRecalls & reported problems across all models
Cardinal Health, Inc. · 164 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Monoject models — page 2
164 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Monoject 8936PG2Container, sharps2 reports
- Monoject 8935YContainer, sharps2 reports
- Monoject 8881401049NEEDLE, DENTAL1 report
- Monoject 1188818100Needle, hypodermic, single lumen1 report
- Monoject 1188822112Needle, hypodermic, single lumen1 report
- Monoject 1188827012Needle, hypodermic, single lumen1 report
- Monoject 8881401171NEEDLE, DENTAL1 report
- Monoject 1180322100Syringe, piston1 report
- Monoject 1180325100Syringe, piston1 report
- Monoject 8881202355CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- Monoject 8881305117NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE1 report
- Monoject 8881225245Tubes, vacuum sample, with anticoagulant1 report
- Monoject 8881225299Catheter,intravascular,therapeutic,short-term less than 30 days1 report
- Monoject 8881516937Syringe, piston1 report
- Monoject 8881907102CONTAINER, LIQUID MEDICATION, GRADUATED1 report
- Monoject 8881500014Syringe, piston1 report
- Monoject 8970Needle, hypodermic, single lumen1 report
- Monoject 8881247137NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE1 report
- Monoject 1522SAContainer, sharps1 report
- Monoject 8881540101Needle, hypodermic, single lumen1 report
- Monoject 8881541307Needle, hypodermic, single lumen1 report
- Monoject 401SGCONTAINER, LIQUID MEDICATION, GRADUATED1 report
- Monoject 1180327114ESYRINGE, PERIODONTIC, ENDODONTIC, IRRIGATING1 report
- Monoject 406SEEnteral Syringes with enteral specific connectors1 death1 report
- Monoject 1182310Needle, hypodermic, single lumen1 report
- Monoject 1181810Needle, hypodermic, single lumen1 report
- Monoject 1181910Needle, hypodermic, single lumen1 report
- Monoject 1182734Needle, hypodermic, single lumen1 report
- Monoject 11811022FCannula, Surgical, General & Plastic Surgery1 report
- Monoject 8881103015Enteral Syringes with enteral specific connectors1 report
- Monoject 8881112015Enteral Syringes with enteral specific connectors1 report
- Monoject 8881520657Syringe, piston1 report
- Monoject 8881513223Syringe, piston1 report
- Monoject 8881512852Syringe, piston1 report
- Monoject 8881512878Syringe, piston1 report
- Monoject 8881535770Syringe, Irrigating (Non Dental)1 report
- Monoject 8881535796Syringe, piston1 report
- Monoject 8881560141Syringe, piston1 report
- Monoject 8881513033Syringe, piston1 report
- Monoject 8881513058Syringe, piston1 report
- Monoject 8881513512Syringe, piston1 report
- Monoject 8881250289Needle, hypodermic, single lumen1 report
- Monoject 8881250313Needle, hypodermic, single lumen1 report
- Monoject 8881501368Syringe, piston1 report
- Monoject 8881511201Syringe, piston1 report
- Monoject 8881511344Syringe, piston1 report
- Monoject 8881541067Needle, hypodermic, single lumen1 report
- Monoject 8881250016Needle, hypodermic, single lumen1 report
- Monoject 8985PG2YContainer, sharps1 report
- Monoject 8881401064NEEDLE, DENTAL1 report
- Monoject 8881200011Needle, hypodermic, single lumen1 report
- Monoject 8881200037Needle, hypodermic, single lumen1 report
- Monoject 8881200060Needle, hypodermic, single lumen1 report
- Monoject 8881200318Needle, hypodermic, single lumen1 report
- Monoject 8881200573Needle, hypodermic, single lumen1 report
- Monoject 8881600350Syringe, piston1 report
- Monoject 8980Container, sharps1 report
- Monoject 8991Container, sharps1 report
- Monoject 8980YContainer, sharps1 report
- Monoject 8997PG2Container, sharps1 report
- Monoject 8997SContainer, sharps1 report
- Monoject 8989Container, sharps1 report
- Monoject 8934Container, sharps1 report
- Monoject 8939Container, sharps1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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