Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 3, 2018
The Shockwave S4 IVL Catheters are intended for lithotripsy-enhanced balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature, including the iliac, femoral, ilio-femoral, popliteal, infra-popliteal, and renal arteries. Shockwave S4, Peripheral Intravascular Lithotripsy Catheter, CE 0086, STERILE R, Manufacturer: Shockwave Medical, Inc. 48501 Warm Springs Blvd. Ste. 108, Fremont, CA 94539
Catheter unable to maintain inflation pressure during treatment (4ATM) and/or during IVL post dilatation (at 6ATM).
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Shockwave Medical, Inc. recalled The Shockwave S4 IVL Catheters are intended for lithotripsy-enhanced balloon dilatation o… - a moderate-severity action.
The Shockwave S4 IVL Catheters are intended for lithotripsy-enhanced balloon dilatation o… was recalled by Shockwave Medical, Inc. in October 3, 2018. Reason: Catheter unable to maintain inflation pressure during treatment (4ATM) and/or during IVL post dilatation (at …. Check the official notice for the remedy. Verify recall #Z-3247-2018 with the FDA Devices before acting.
The recall
Shockwave Medical, Inc. issued this moderate-severity FDA Devices recall-Catheter unable to maintain inflation pressure during treatment (4ATM) and/or during IVL post dilatation (at ….
- Moderate
- severity level
- 612 units
- affected scope
- Class II
- classification
- October 3, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-3247-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-3247-2018) was formally reported on October 3, 2018, with the manufacturer initiating the action on July 18, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Shockwave Medical, Inc. is listed as the recalling firm, operating out of Fremont, CA. Federal records list the affected scope as 612.
The documented reason for this recall is: Catheter unable to maintain inflation pressure during treatment (4ATM) and/or during IVL post dilatation (at 6ATM). Distribution data in the federal record shows the product reached: Domestic: CO, TN and TX Foreign: Austria, Germany and New Zealand. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,422 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
612
Related Recalls
6
0 from same agency
Product description
The Shockwave S4 IVL Catheters are intended for lithotripsy-enhanced balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature, including the iliac, femoral, ilio-femoral, popliteal, infra-popliteal, and renal arteries. Shockwave S4, Peripheral Intravascular Lithotripsy Catheter, CE 0086, STERILE R, Manufacturer: Shockwave Medical, Inc. 48501 Warm Springs Blvd. Ste. 108, Fremont, CA 94539
Reason for recall
Catheter unable to maintain inflation pressure during treatment (4ATM) and/or during IVL post dilatation (at 6ATM).
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-3247-2018 |
| Date reported | October 3, 2018 |
| Date initiated | July 18, 2018 |
| Recalling firm | Shockwave Medical, Inc. |
| Firm location | Fremont, CA |
| Affected scope | 612 |
| Distribution | Domestic: CO, TN and TX Foreign: Austria, Germany and New Zealand |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-3247-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
The Shockwave S4 IVL Catheters are intended for lithotripsy-enhanced balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature, including the iliac, femoral, ilio-femoral, popliteal, infra-popliteal, and renal arteries. Shockwave S4, Peripheral Intravascular Lithotripsy Catheter, CE 0086, STERILE R, Manufacturer: Shockwave Medical, Inc. 48501 Warm Springs Blvd. Ste. 108, Fremont, CA 94539. Recalled by Shockwave Medical, Inc.. Units affected: 612.
Why was this product recalled? ▼
Catheter unable to maintain inflation pressure during treatment (4ATM) and/or during IVL post dilatation (at 6ATM).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 3, 2018. Severity: Moderate. Recall number: Z-3247-2018.
Where was the recalled product distributed? ▼
Distribution: Domestic: CO, TN and TX Foreign: Austria, Germany and New Zealand.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-3247-2018) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported October 3, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.