CLASS III Device recall · Reported 1 Mar 2017 · FDA Enforcement Report
AMT Right Angle Feeding Set with Y-Port Used recalled
Applied Medical Technology is recalling AMT Right Angle Feeding Set with Y-Port Used with Nasogastric/Nasointestinal (NG/NI) tubes, distributed in 20 states. The recall was initiated on 19 Jan 2017 and the FDA has classified it as Class III.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1224-2017
- FDA event ID
- 76264
- Recalling firm
- Applied Medical Technology, Brecksville, OH
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 19 Jan 2017
- FDA classified
- 17 Feb 2017
- Reported
- 1 Mar 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 19 Jan 2017 | Recall initiated by company | |
| 17 Feb 2017 | Classified by FDA | +29 days |
| 1 Mar 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Expired expiration dates are listed on the pouches.
Product as listed by the FDA
AMT 12 inch Right Angle Feeding Set with Y-Port Used with Nasogastric/Nasointestinal (NG/NI) tubes.
Where it was distributed
US Distribution to the states of : AZ, CA, CO, CT, FL, GA, ID, LA, ME, MO, MN, NC, OH, OK, OR, TN, TX, UT, WA, and WI., and to the United Kingdom.
ArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIdahoLouisianaMaineMinnesotaMissouriNorth CarolinaOhioOklahomaOregonTennesseeTexasUtahWashingtonWisconsin
Questions about this recall
Why was it recalled?
Expired expiration dates are listed on the pouches.
Which lots are affected?
Table 5: 8-1222 Box P/N - 8-1222 Box Lot Number - 161003-312 Box Exp. - 2019-09-01 Box UDI - (01)00842071108649(17)190901(10)161003-312 Pouch P/N - E8-1222 Pouch Lot Number - 160923-222 Pouch Exp. - 2016-09-01 Pouch UDI - (01)00842071107536(17)160901(10)160923-222
Where was it sold?
US Distribution to the states of : AZ, CA, CO, CT, FL, GA, ID, LA, ME, MO, MN, NC, OH, OK, OR, TN, TX, UT, WA, and WI., and to the United Kingdom.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 76264| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS III | AMT Bridle - Nasal Tube Retaining System Used recalled | Applied Medical Technology | Other | 20 states |
More recalls from Applied Medical Technology
All 19| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS II | NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS II | NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS II | NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS II | NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
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