Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29406 |
| Brand Name: | Medline Custom Procedure Kits Class 2a |
| Model: | Pack Code: CSBANZSG01A, CSOPNZSG08A, SBANZAH06K, SBANZAH06M, SCVNZAH02M, SCVNZAH03I, SCVNZAH05G, SCVNZAH06F, SCVNZAH06G, SENNZAH03H, SENNZAH03I, SENNZAH09I, SOPNZSQ02E |
| Affected: | CD2142075, CD2142212, CD2142083, CD2142234, CS2115178, CS2199678, CS2117067, CS2117223, CS2120378, CS2100471, CS2102283, CS2118261, CS2120104, CS2120569, CS2105935, CS2107874, CS2113329, CS2116501, CS2119992, CS2112342, CS2117632, CS2112262, CS2116510 |
| Software version: | |
| Recalling Organisation: | Paragon Care Group New Zealand Limited 69 Elizabeth Knox Place Glen Innes AUCKLAND |
| Contact Information: | 0508 654 258 |
| Manufacturer: | Medline Assembly Australia Pty Ltd |
| Issue: | The manufacturer has received complaints reporting an observation of air in damaged syringes for BD Plastipak ™ 50mL Syringe with Luer? Lok™ Tip. When a damaged barrel syringe is used with a syringe pump, there is a possibility that ingress of air into the syringe could potentially inject air into the vascular system. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/5/2022 |
