NEOMED*Recalls & reported problems across all models
Avanos Medical, Inc. · 24 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
3 open recalls name at least one NEOMED* model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 3
We found 24 models of NEOMED* by Avanos Medical, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
3 FDA recall records name at least one of these models by its device identifier, 3 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
NEOMED* recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Mar 4, 2024Open, Classified
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
Z-2037-2024 · Root cause: Under Investigation by firm · names 8 of these models · Recall details · FDA record ↗
- Mar 4, 2024Open, Classified
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
Z-2036-2024 · Root cause: Under Investigation by firm · names 8 of these models · Recall details · FDA record ↗
- Mar 4, 2024Open, Classified
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
Z-2035-2024 · Root cause: Under Investigation by firm · names 8 of these models · Recall details · FDA record ↗
NEOMED* models
24 models, most reported first. Each model has its own page with its reports, recalls and device details.
- NEOMED* BA-S05EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BA-S1EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BA-S3EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BA-S6EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BA-S12EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BA-S20EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BA-S35EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BA-S60EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S05EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S1EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S3EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S6EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S12EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S20EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S35EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BC-S60EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S05EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S1EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S3EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S6EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S12EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S20EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S35EODISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S60EODISPENSER, LIQUID MEDICATION1 recall0 reports
Other Avanos Medical, Inc. products
- Halyard232 models · 1,210 reports · 1 recall
- Ballard* Closed Suction System30 models · 340 reports · 2 recalls
- Ballard* Turbo-Cleaning Closed Suction System16 models · 123 reports · 3 recalls
- Ballard* Closed Suction System for Adults17 models · 121 reports · 3 recalls
- CORTRAK* 2 Enteral Access System2 models · 134 reports · 1 recall
- Cortrak 2 Enternal access device14 models · 164 reports
- Microcuff* Endotracheal Tube for Adults8 models · 102 reports
- ON-Q* Pain Relief System with SELECT-A-FLOW*2 models · 94 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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