Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported May 31, 2017
Pointe Scientific Chemistry Controls Level I and II LEVl: Amber glass vial w/PP white plastic cap. LEV2: Amber glass vial w/PP black plastic cap.
The original mean assigned to the control too high, upon reassignment with additional data the new assigned mean was outside of the originally published range.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Medtest Holdings, Inc. recalled Pointe Scientific Chemistry Controls Level I and II LEVl: Amber glass vial w/PP white … - a low-severity action.
Pointe Scientific Chemistry Controls Level I and II LEVl: Amber glass vial w/PP white … was recalled by Medtest Holdings, Inc. in May 31, 2017. Reason: The original mean assigned to the control too high, upon reassignment with additional data the new assigned m…. Check the official notice for the remedy. Verify recall #Z-2121-2017 with the FDA Devices before acting.
The recall
Medtest Holdings, Inc. issued this low-severity FDA Devices recall-The original mean assigned to the control too high, upon reassignment with additional data the new assigned m….
- Low
- severity level
- Class III
- classification
- May 31, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2121-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2121-2017) was formally reported on May 31, 2017, with the manufacturer initiating the action on May 15, 2014. It is classified under Low severity (Class III), with a current status of Terminated. Medtest Holdings, Inc. is listed as the recalling firm, operating out of Canton, MI. Federal records list the affected scope as 132919 Vol vials.
The documented reason for this recall is: The original mean assigned to the control too high, upon reassignment with additional data the new assigned mean was outside of the originally published range. Distribution data in the federal record shows the product reached: Nationwide. 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, 3 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 - 40,322 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
132919 Vol vials
Related Recalls
6
3 from same agency
Product description
Pointe Scientific Chemistry Controls Level I and II LEVl: Amber glass vial w/PP white plastic cap. LEV2: Amber glass vial w/PP black plastic cap.
Reason for recall
The original mean assigned to the control too high, upon reassignment with additional data the new assigned mean was outside of the originally published range.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-2121-2017 |
| Date reported | May 31, 2017 |
| Date initiated | May 15, 2014 |
| Recalling firm | Medtest Holdings, Inc. |
| Firm location | Canton, MI |
| Affected scope | 132919 Vol vials |
| Distribution | Nationwide |
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-2121-2017) 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? ▼
Pointe Scientific Chemistry Controls Level I and II LEVl: Amber glass vial w/PP white plastic cap. LEV2: Amber glass vial w/PP black plastic cap.. Recalled by Medtest Holdings, Inc.. Units affected: 132919 Vol vials.
Why was this product recalled? ▼
The original mean assigned to the control too high, upon reassignment with additional data the new assigned mean was outside of the originally published range.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 31, 2017. Severity: Low. Recall number: Z-2121-2017.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2121-2017) 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.
Nearby Recalls in This Category
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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 May 31, 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.