Medimop Vial2Bag DC Recall: IV Port May Separate During Drug Reconstitution
Medimop recalls specific lots of Vial2Bag DC devices due to risk of IV port separating during drug reconstitution. Affected units include lots 9507-9513. Contact for remedy details.
Use caution until it’s fixed
Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag DC body during the drug reconstitution I IV Set attachment process.
Contact the company
What happened, in plain English
Medimop is recalling certain lots of Vial2Bag DC devices because the IV port might detach while attaching IV sets during drug preparation. This could lead to medication errors or injury if the port separates during use. Read more at govinfonow.com/recall/72898-medimop-vial2bag-dc-recall-iv-port-may-separate-during-drug.
Source Summary by GovInfoNow · govinfonow.com/recall/72898-medimop-vial2bag-dc-recall-iv-port-may-separate-during-drug · Updated September 17, 2026 · FDA enforcement record: FDA #Z-0972-2018
Cite this page
“Medimop Vial2Bag DC Recall: IV Port May Separate During Drug Reconstitution.” GovInfoNow, updated September 17, 2026. https://govinfonow.com/recall/72898-medimop-vial2bag-dc-recall-iv-port-may-separate-during-drug. Based on FDA recall #Z-0972-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0972-2018%22&limit=1).
Why it’s dangerous
The IV port may separate from the Vial2Bag DC body when attaching IV sets during drug reconstitution. This could cause medication errors or injury if the port detaches while the device is in use.
Who’s affected
Healthcare workers and patients using the device in home or clinical settings. Those with specific lot numbers (9507-9513) are most at risk.
How to tell if you have this one
Check the product lot number on the device. Affected lots are 950: 9507, 9508, 9509, 9510, 9511, 9512, 9513. The device is used for drug reconstitution in healthcare or home settings.
- Brand
Medimop- Category
Medical device
What to do — step by step
Check Lot Number
Identify the lot number on the device, which should be one of 9507-9513.
How this recall unfolded
Recall timeline
FDA terminated this recall 6.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0972-2018 (October 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0972-2018 to see it in context.
- Plain-language summary written by qwen3:4b on September 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.