Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported August 2, 2017
PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory in Newborn Screening.
PerkinElmer 226 Sample Collection Devices Lot Number 317114 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained withi…
Compiled from official public sources by the editorial team.
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PerkinElmer Health Sciences, Inc. recalled PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device … - a low-severity action.
PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device … was recalled by PerkinElmer Health Sciences, Inc. in August 2, 2017. Reason: PerkinElmer 226 Sample Collection Devices Lot Number 317114 had serial numbers printed on the pack labels tha…. Check the official notice for the remedy. Verify recall #Z-2756-2017 with the FDA Devices before acting.
The recall
PerkinElmer Health Sciences, Inc. issued this low-severity FDA Devices recall-PerkinElmer 226 Sample Collection Devices Lot Number 317114 had serial numbers printed on the pack labels tha….
- Low
- severity level
- 100K units
- affected scope
- Class III
- classification
- August 2, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2756-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2756-2017) was formally reported on August 2, 2017, with the manufacturer initiating the action on May 31, 2017. It is classified under Low severity (Class III), with a current status of Terminated. PerkinElmer Health Sciences, Inc. is listed as the recalling firm, operating out of Greenville, SC. Federal records list the affected scope as 99,968 units.
The documented reason for this recall is: PerkinElmer 226 Sample Collection Devices Lot Number 317114 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack. Distribution data in the federal record shows the product reached: US Distribution to the state of : AL. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
99,968 units
Related Recalls
6
0 from same agency
Product description
PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory in Newborn Screening.
Reason for recall
PerkinElmer 226 Sample Collection Devices Lot Number 317114 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-2756-2017 |
| Date reported | August 2, 2017 |
| Date initiated | May 31, 2017 |
| Recalling firm | PerkinElmer Health Sciences, Inc. |
| Firm location | Greenville, SC |
| Affected scope | 99,968 units |
| Distribution | US Distribution to the state of : AL |
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-2756-2017) 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? ▼
PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory in Newborn Screening.. Recalled by PerkinElmer Health Sciences, Inc.. Units affected: 99,968 units.
Why was this product recalled? ▼
PerkinElmer 226 Sample Collection Devices Lot Number 317114 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 2, 2017. Severity: Low. Recall number: Z-2756-2017.
Where was the recalled product distributed? ▼
Distribution: US Distribution to the state of : AL.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2756-2017) 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 August 2, 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.