Browse Device Recalls
19 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 19 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Medical Device Recalls
Browse 19 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Oct 6, 2025 | Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tub... | The nasal feeding tube may be occluded | Class II | Applied Medical Technology Inc |
| Oct 6, 2025 | Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tub... | The nasal feeding tube may be occluded | Class II | Applied Medical Technology Inc |
| Oct 6, 2025 | Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tub... | The nasal feeding tube may be occluded | Class II | Applied Medical Technology Inc |
| Oct 6, 2025 | Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tub... | The nasal feeding tube may be occluded | Class II | Applied Medical Technology Inc |
| Oct 6, 2025 | Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tub... | The nasal feeding tube may be occluded | Class II | Applied Medical Technology Inc |
| Aug 12, 2025 | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NR... | The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at l... | Class II | Applied Medical Technology Inc |
| Aug 12, 2025 | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NR... | The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at l... | Class II | Applied Medical Technology Inc |
| Aug 12, 2025 | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NR... | The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at l... | Class II | Applied Medical Technology Inc |
| Aug 12, 2025 | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NR... | The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at l... | Class II | Applied Medical Technology Inc |
| Nov 26, 2024 | AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Mode... | The extension sets subject to this recall have ENFit connections, although they should have non- ... | Class II | Applied Medical Technology Inc |
| May 14, 2024 | AMT Initial Placement Dilator Set. Used to place gastrostomy devices. | Devices were labelled with the incorrect guidewire labelling. | Class II | Applied Medical Technology Inc |
| Nov 10, 2020 | AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102... | The products subject to this recall may contain obvious, incorrect pouch labels while the outer b... | Class III | Applied Medical Technology Inc |
| Jan 19, 2017 | AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointesti... | Expired expiration dates are listed on the pouches. | Class III | Applied Medical Technology Inc |
| Jan 19, 2017 | AMT 12 inch Right Angle Feeding Set with Y-Port Used with Nasogastric/Naso... | Expired expiration dates are listed on the pouches. | Class III | Applied Medical Technology Inc |
| Feb 17, 2016 | TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STA... | The firm received a complaint of an open pouch which breaches the sterilization validation. | Class II | Applied Medical Technology Inc |
| Feb 17, 2016 | Wilson Implantation System Product Usage: Indicated to aid in tissue retr... | The firm received a complaint of an open pouch which breaches the sterilization validation. | Class II | Applied Medical Technology Inc |
| Feb 17, 2016 | TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) STERILE EO... | The firm received a complaint of an open pouch which breaches the sterilization validation. | Class II | Applied Medical Technology Inc |
| Feb 17, 2016 | Wilson Penile Implantation System Retractor Frame, Retractor Stays & Penile E... | The firm received a complaint of an open pouch which breaches the sterilization validation. | Class II | Applied Medical Technology Inc |
| Jan 26, 2016 | AMT G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SIN... | The firm received complaints that the product is shorter in length than indicated on the label. | Class II | Applied Medical Technology Inc |
Frequently Asked Questions
When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.
All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.
Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.