Recall Register

Food, drugs, devices › Firms

BALT USA, LLC

FDA recalling firm · 6 enforcement events · 8 product records · 2022–2025 · CA

BALT USA, LLC has 6 FDA enforcement events on this register (8 product records) between 2022 and 2025: 6 device; the busiest year was 2022 with 3.

17% of its events are Class I; the most common class is Class II (5). 6 events are listed as ongoing; the recalling firm's address is in CA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
25 Sep 2025Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Ballast Model/Catalog Number: MEGABT09180, MEGABT09190, MEGABT091100, MEGABT091110 Software Version: N/A Product Description: The Mega Ballast 091 is designed with a semi-rigid proximal shaft and a highly flexible distal shaft. The design facilitates…DeviceClass I1Ongoing
8 May 2025Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851 OPTI0258BLK 00810068568929 OPTI0212BLK 00810068568912 OPTI0206BLK 00810068568905 OPTI0310BLK 00810068568943 OPTI0320BLK 00810068568950 OPTI0151HSS10 00818053026614 OPTI0152HSS10 00840303701002…DeviceClass II2Ongoing
3 Jan 2024Neurovascular embolization device. The Optima Coil System is a series specialized coils that are inserted into the vasculature under angiographic visualization to embolize intracranial aneurysms and other vascular anomalies. The system consists of an embolization coil implant comprised of platinum/tungsten, affixed…DeviceClass II2Ongoing
7 Sep 2022Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovascular procedures.DeviceClass II1Ongoing
26 Jul 2022Optima Coil System Model OPTI0520CSF10. For endovascular embolization.DeviceClass II1Ongoing
4 Jan 2022The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to a proximal stainless steel hypo-tube and distal body coil delivery pusher with a radiopaque distal positioning marker and proximal fluorosafe marker. The Optima Coil delivery pusher is 185cm in…DeviceClass II1Ongoing

By type and class

Device6
Class II5
Class I1

Class I: 17% of this firm's events; 18% of all events on the register.

Events by year

22
23
24
25
26
Enforcement events for BALT USA, LLC by year initiated.

Questions and answers

How many FDA recalls has BALT USA, LLC had?

6 enforcement events (8 product records) on this register, 2022–2025: 6 device.

Are any BALT USA, LLC recalls ongoing?

6 events are listed as ongoing in the current openFDA export.

What class are BALT USA, LLC recalls?

5 Class II, 1 Class I. 17% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.