CLASS II Device recall · Reported 20 Apr 2016 · FDA Enforcement Report
Amt G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device recalled
Applied Medical Technology is recalling Amt G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F Single Use Only, distributed in 8 states. The recall was initiated on 26 Jan 2016 and the FDA has classified it as Class II.
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-1497-2016
- FDA event ID
- 73339
- Recalling firm
- Applied Medical Technology, Brecksville, OH
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Jan 2016
- FDA classified
- 14 Apr 2016
- Reported
- 20 Apr 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 26 Jan 2016 | Recall initiated by company | |
| 14 Apr 2016 | Classified by FDA | +79 days |
| 20 Apr 2016 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The firm received complaints that the product is shorter in length than indicated on the label.
Product as listed by the FDA
AMT G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE. For use in patients who cannot absorb adequate nutrition through the stomach.
Where it was distributed
Distributed in the states of AZ, CA, DE, IN, MI, NM, PA & VA.
ArizonaCaliforniaDelawareIndianaMichiganNew MexicoPennsylvaniaVirginia
Questions about this recall
Why was it recalled?
The firm received complaints that the product is shorter in length than indicated on the label.
Which lots are affected?
Model #GJ-1415-45, Lot # 15104750, Exp Date: 2018/09
Where was it sold?
Distributed in the states of AZ, CA, DE, IN, MI, NM, PA & VA.
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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.
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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