See Luer Cap Set, MPC-130, set, administration, intravascular
FDA device recall Z-1774-2026 · posted 2026-04-06 · Open, Classified
Recall details
- Recalling firm
- Molded Products Inc
- Reason for recall
- Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.
- Action taken
- Molded Products, Inc. issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 02/17/2026 via USPS First Class Mail. The notice explained the issue and requested the following: Please take the following actions: 1. Please inspect your inventory to determine if you have any of the affected lot. Quarantine the affected product and initiate a return to Molded Products, Inc. for credit. 2. Share this recall notification will all users of the product to ensure they are also aware of this recall. 3. Complete the attached Medical Device Recall Customer Response Form and return to the contact noted below whether or not you have any of the impacted material so that Molded Products may acknowledge your receipt of this notification and process your return and credit. For complaints, adverse events, or questions, contact Teresa Wooster, twooster@moldedproducts.com; Ph# 800-435-8957 ext. 236 Monday Friday 8:00am-4:30pm (CT), Fax# 800-227-7935.
- Root cause
- Process control
- Status
- Open, Classified
- Product code
- FPA
- Quantity affected
- 26900 units
- Distribution
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
- Date initiated
- 2026-02-17
- Date posted
- 2026-04-06
- Location
- Harlan, IA
Monitor recalls programmatically
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MPC-1000 INJECTION CAP/PLUG (K925927) | Molded Products, Inc. | 1993-08-16 |