PlainRecalls
CriticalClass IOngoing

FDA Devices recall · Reported April 1, 2020

Imager II 5F Angiographic Catheters, 5 units per package.

Potential for tip detachment of Imager II 5F Angiographic Catheters

Recall #
Z-1555-2020
Affected scope
1068827 Single Units
Initiated
February 11, 2020
Verify with FDA Devices →
View my saved recalls

Boston Scientific Corporation recalled Imager II 5F Angiographic Catheters, 5 units per package. - a critical-severity action.

Imager II 5F Angiographic Catheters, 5 units per package. was recalled by Boston Scientific Corporation in April 1, 2020. Reason: Potential for tip detachment of Imager II 5F Angiographic Catheters. Check the official notice for the remedy. Verify recall #Z-1555-2020 with the FDA Devices before acting.

The recall

Boston Scientific Corporation issued this critical-severity FDA Devices recall-Potential for tip detachment of Imager II 5F Angiographic Catheters.

Critical
severity level
Class I
classification
April 1, 2020
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-1555-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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, 6 from FDA Devices - 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 - 41,021 medical devices recalls on record

01,0002,0003,0004,000 20052008201120142017202020232026 1,947
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Imager II 5F Angiographic Catheters, 5 units per package.

Reason for recall

Potential for tip detachment of Imager II 5F Angiographic Catheters

Recall Profile

Structured summary of the FDA Devices recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Ongoing
Recall number Z-1555-2020
Date reported April 1, 2020
Date initiated February 11, 2020
Recalling firm Boston Scientific Corporation
Firm location Maple Grove, MN
Affected scope 1068827 Single Units
Distribution Worldwide distribution. US nationwide, Australia, Belgium, Brazil, Canada, Switzerland, China, Colombia, Cyprus, Czech Republic, Germany, Spain, Finland, France, Great Britain, Greece, Croatia, Hungary, Indonesia, Israel, India, Italy, Jo…

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-1555-2020) 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.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. 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?
Imager II 5F Angiographic Catheters, 5 units per package.. Recalled by Boston Scientific Corporation. Units affected: 1068827 Single Units.
Why was this product recalled?
Potential for tip detachment of Imager II 5F Angiographic Catheters
Which agency issued this recall?
This recall was issued by the FDA Devices on April 1, 2020. Severity: Critical. Recall number: Z-1555-2020.
Where was the recalled product distributed?
Distribution: Worldwide distribution. US nationwide, Australia, Belgium, Brazil, Canada, Switzerland, China, Colombia, Cyprus, Czech Republic, Germany, Spain, Finland, France, Great Britain, Greece, Croatia, Hungary, Indonesia, Israel, India, Italy, Jordan, Japan, South Korea, Lebanon, Lithuania, Mexico, Malaysia, Netherlands, Norway, Poland, Russia, Sweden, Slovakia, Turkey, Taiwan, and South Africa..
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.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Compare this recall with GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VS… → · All Medical Devices recalls

This recall: FDA Devices, reported April 1, 2020. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026