BD Insyte Autoguard Catheter An active safety engineered peripheral… — Class II medical device recall Z-0572-2015
Terminated recall by Becton Dickinson & Company, reported 2014-12-17. BD Insyte Autoguard may have potential damage along the body of the catheter.
| Recall number | Z-0572-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2014-10-09 |
| Classified | 2014-12-09 |
| Reported by FDA | 2014-12-17 |
| Terminated | 2015-04-24 |
| Countries outside the US | CA, CR, ES, IT, JP, MX, PA, PE, ZA |
| Lot numbers | 4105724, 4107722, 4113707, 4113713, 4119700, 4119730, 4129576, 4139786, 4143917, 4147742, 4161662, 4164960, 4167812, 4174713, 4182668, APR-17, JUL-17, JUN-17, MAY-17 |
| Model numbers | 1.00, 1.16, 3811834, 381433, 381434, 381833 |
Product
BD Insyte Autoguard Catheter An active safety engineered peripheral IV catheter with a retracting needle to reduce accidental needle stick injuries. The safety feature (needle retraction) of this device is activated when the clinician depresses the button located on the superior surface of the grip. This product is used to provide access to the intravascular system for administration of fluids, medication, blood and blood products and for the withdrawal of the blood samples.
Reason for recall
BD Insyte Autoguard may have potential damage along the body of the catheter.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0572-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.