FDA Medical Device Recalls (openFDA)
Molded Products Inc: See Luer Cap Set, MPC-130, set, administration, intravascular
- Recall number
- Z-1774-2026
- Recalling firm
- Molded Products Inc
- Product
- See Luer Cap Set, MPC-130, set, administration, intravascular
- Status
- Open, Classified
- Initiated
- 2026-02-17
- Posted
- 2026-04-06
- Terminated
- not on file
- Reason
- 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.
- Root cause
- Process control
- Action
- 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.
- Quantity
- 26900 units
- Distribution
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
- Lot, serial or model codes
- UDI +B144MPC1300/$$529105203895, Lot Number 20389
- 510(k) numbers
- ["K925927"]
- PMA numbers
- not on file
- Product code
- FPA
- Firm FEI
- 1000138417
- Firm city
- Harlan
- Firm state
- IA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28