Severity
Critical
CriticalClass ITerminated
FDA Devices recall · Reported December 14, 2022
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST
An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Remel Inc recalled Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST - a critical-severity action.
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST was recalled by Remel Inc in December 14, 2022. Reason: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Pl…. Check the official notice for the remedy. Verify recall #Z-0328-2023 with the FDA Devices before acting.
The recall
Remel Inc issued this critical-severity FDA Devices recall-An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Pl….
- Critical
- severity level
- 2K units
- affected scope
- Class I
- classification
- December 14, 2022
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0328-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0328-2023) was formally reported on December 14, 2022, with the manufacturer initiating the action on October 20, 2022. It is classified under Critical severity (Class I), with a current status of Terminated. Remel Inc is listed as the recalling firm, operating out of Lenexa, KS. Federal records list the affected scope as 2471 units.
The documented reason for this recall is: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morgane… Distribution data in the federal record shows the product reached: US Nationwide Distribution. 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
2471 units
Related Recalls
6
3 from same agency
Product description
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST
Reason for recall
An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | Z-0328-2023 |
| Date reported | December 14, 2022 |
| Date initiated | October 20, 2022 |
| Recalling firm | Remel Inc |
| Firm location | Lenexa, KS |
| Affected scope | 2471 units |
| Distribution | US Nationwide Distribution |
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-0328-2023) 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? ▼
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST. Recalled by Remel Inc. Units affected: 2471 units.
Why was this product recalled? ▼
An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 14, 2022. Severity: Critical. Recall number: Z-0328-2023.
Where was the recalled product distributed? ▼
Distribution: US Nationwide Distribution.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0328-2023) 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 December 14, 2022. 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.