Recall Z-0365-2020— Cadence Science, Inc.
Class II · Terminated
Class II FDA medical device recall by Cadence Science, Inc., initiated 2019-05-10, terminated 2020-06-05. FDA's recall record names no specific 510(k) clearance for this event. Product: Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404); 5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use. Reason: The glass syringe used with Pressure Control Syringes may potentially break during use..
- Recalling firm
- Cadence Science, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-05-10
- Terminated
- 2020-06-05
- Firm location
- Cranston, RI, United States
Product description
Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404); 5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use
Reason for recall
The glass syringe used with Pressure Control Syringes may potentially break during use.
Data sourced from openFDA. This site is unofficial and independent of the FDA.