Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 4, 2017
NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes), Sterile, Rx.. Manufactured for: Novadaq Technologies Inc., Burnaby, BC, Canada. The SPY-PHI Drape is intended to cover the SPY-PHI System to maintain a sterile field, and as an aid in the clean-up of equipment after surgery or other medical procedures. The product is not intended to be used as patient drapes and they have no patient contact.
The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Novadaq Technologies INC. recalled NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes)… - a moderate-severity action.
NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes)… was recalled by Novadaq Technologies INC. in October 4, 2017. Reason: The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the ster…. Check the official notice for the remedy. Verify recall #Z-3236-2017 with the FDA Devices before acting.
The recall
Novadaq Technologies INC. issued this moderate-severity FDA Devices recall-The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the ster….
- Moderate
- severity level
- Class II
- classification
- October 4, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-3236-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-3236-2017) was formally reported on October 4, 2017, with the manufacturer initiating the action on June 27, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Novadaq Technologies INC. is listed as the recalling firm, operating out of Burnaby, N/A. Federal records list the affected scope as 3/20-drape boxes.
The documented reason for this recall is: The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier. Distribution data in the federal record shows the product reached: Worldwide Distribution. US (nationwide) to states of: CA, CO, ID, IL, NY, OR, and VA; and countries of: Canada, Belgium, and Lithuania.. 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
3/20-drape boxes
Related Recalls
6
0 from same agency
Product description
NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes), Sterile, Rx.. Manufactured for: Novadaq Technologies Inc., Burnaby, BC, Canada. The SPY-PHI Drape is intended to cover the SPY-PHI System to maintain a sterile field, and as an aid in the clean-up of equipment after surgery or other medical procedures. The product is not intended to be used as patient drapes and they have no patient contact.
Reason for recall
The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-3236-2017 |
| Date reported | October 4, 2017 |
| Date initiated | June 27, 2017 |
| Recalling firm | Novadaq Technologies INC. |
| Firm location | Burnaby, N/A |
| Affected scope | 3/20-drape boxes |
| Distribution | Worldwide Distribution. US (nationwide) to states of: CA, CO, ID, IL, NY, OR, and VA; and countries of: Canada, Belgium, and Lithuania. |
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-3236-2017) 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? ▼
NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes), Sterile, Rx.. Manufactured for: Novadaq Technologies Inc., Burnaby, BC, Canada. The SPY-PHI Drape is intended to cover the SPY-PHI System to maintain a sterile field, and as an aid in the clean-up of equipment after surgery or other medical procedures. The product is not intended to be used as patient drapes and they have no patient contact.. Recalled by Novadaq Technologies INC.. Units affected: 3/20-drape boxes.
Why was this product recalled? ▼
The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 4, 2017. Severity: Moderate. Recall number: Z-3236-2017.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution. US (nationwide) to states of: CA, CO, ID, IL, NY, OR, and VA; and countries of: Canada, Belgium, and Lithuania..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-3236-2017) 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 4, 2017. 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.