Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported September 11, 2019
Norm-O-Temp model 111Z
The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tissue damage.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Cincinnati Sub-Zero Products LLC, a Gentherm Company recalled Norm-O-Temp model 111Z - a moderate-severity action.
Norm-O-Temp model 111Z was recalled by Cincinnati Sub-Zero Products LLC, a Gentherm Company in September 11, 2019. Reason: The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tiss…. Check the official notice for the remedy. Verify recall #Z-2355-2019 with the FDA Devices before acting.
The recall
Cincinnati Sub-Zero Products LLC, a Gentherm Company issued this moderate-severity FDA Devices recall-The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tiss….
- Moderate
- severity level
- 674 units
- affected scope
- Class II
- classification
- September 11, 2019
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2355-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2355-2019) was formally reported on September 11, 2019, with the manufacturer initiating the action on June 20, 2019. It is classified under Moderate severity (Class II), with a current status of Terminated. Cincinnati Sub-Zero Products LLC, a Gentherm Company is listed as the recalling firm, operating out of Cincinnati, OH. Federal records list the affected scope as 674.
The documented reason for this recall is: The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tissue damage. Distribution data in the federal record shows the product reached: Ship-To State AL AR AZ CA CO CT DC DE FL GA HI IL IN KS KY LA MA MD ME MI MN MO NC ND NE NH NJ NM NY OH OK PA RI SC TN TW TX UT VA WA WI WV WY Ship-To Country United States…. 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 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
674
Related Recalls
6
3 from same agency
Product description
Norm-O-Temp model 111Z
Reason for recall
The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tissue damage.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2355-2019 |
| Date reported | September 11, 2019 |
| Date initiated | June 20, 2019 |
| Recalling firm | Cincinnati Sub-Zero Products LLC, a Gentherm Company |
| Firm location | Cincinnati, OH |
| Affected scope | 674 |
| Distribution | Ship-To State AL AR AZ CA CO CT DC DE FL GA HI IL IN KS KY LA MA MD ME MI MN MO NC ND NE NH NJ NM NY OH OK PA RI SC TN TW TX UT VA WA WI WV WY Ship-To Country United States Taiwan Egypt Uni… |
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-2355-2019) 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? ▼
Norm-O-Temp model 111Z. Recalled by Cincinnati Sub-Zero Products LLC, a Gentherm Company. Units affected: 674.
Why was this product recalled? ▼
The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tissue damage.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 11, 2019. Severity: Moderate. Recall number: Z-2355-2019.
Where was the recalled product distributed? ▼
Distribution: Ship-To State AL AR AZ CA CO CT DC DE FL GA HI IL IN KS KY LA MA MD ME MI MN MO NC ND NE NH NJ NM NY OH OK PA RI SC TN TW TX UT VA WA WI WV WY Ship-To Country United States Taiwan Egypt United Arab Emirates Israel Pakistan Turkey Colombia Thailand Kuwait United Kingdom Mexico Netherlands Canada Ecuador South Korea Germany Georgia China Panama Japan Malaysia Hong Kong Austria Chile Mongolia Morocco Australia Indonesia Venezuela Singapore.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2355-2019) 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 September 11, 2019. 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.