Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported April 8, 2020
Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing.
During an FDA audit, it was discovered that the product was not properly registered with FDA.
Gentell, Inc recalled Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthc… - a moderate-severity action.
Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthc… was recalled by Gentell, Inc in April 8, 2020. Reason: During an FDA audit, it was discovered that the product was not properly registered with FDA.. Check the official notice for the remedy. Verify recall #Z-1625-2020 with the FDA Devices before acting.
The recall
Gentell, Inc issued this moderate-severity FDA Devices recall-During an FDA audit, it was discovered that the product was not properly registered with FDA..
- Moderate
- severity level
- 6K units
- affected scope
- Class II
- classification
- April 8, 2020
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1625-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1625-2020) was formally reported on April 8, 2020, with the manufacturer initiating the action on February 27, 2020. It is classified under Moderate severity (Class II), with a current status of Ongoing. Gentell, Inc is listed as the recalling firm, operating out of Bristol, PA. Federal records list the affected scope as 6,433.
The documented reason for this recall is: During an FDA audit, it was discovered that the product was not properly registered with FDA. Distribution data in the federal record shows the product reached: Worldwide distribution US Nationwide distribution in the states of AL, CA, FL, IA, IL, KY, MA, MI, MN, NC, NJ, NY, OH, OK, PA, Puerto Rico, RI, SC, TN, TX, WI and countries of Panama, South Africa, Bahrain, Spain, Mex…. 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
6,433
Related Recalls
6
3 from same agency
Product description
Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing.
Reason for recall
During an FDA audit, it was discovered that the product was not properly registered with FDA.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1625-2020 |
| Date reported | April 8, 2020 |
| Date initiated | February 27, 2020 |
| Recalling firm | Gentell, Inc |
| Firm location | Bristol, PA |
| Affected scope | 6,433 |
| Distribution | Worldwide distribution US Nationwide distribution in the states of AL, CA, FL, IA, IL, KY, MA, MI, MN, NC, NJ, NY, OH, OK, PA, Puerto Rico, RI, SC, TN, TX, WI and countries of Panama, South Africa, Bahrain, Spain, Mexico, Costa Rica, Rom… |
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-1625-2020) 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? ▼
Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing.. Recalled by Gentell, Inc. Units affected: 6,433.
Why was this product recalled? ▼
During an FDA audit, it was discovered that the product was not properly registered with FDA.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 8, 2020. Severity: Moderate. Recall number: Z-1625-2020.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution US Nationwide distribution in the states of AL, CA, FL, IA, IL, KY, MA, MI, MN, NC, NJ, NY, OH, OK, PA, Puerto Rico, RI, SC, TN, TX, WI and countries of Panama, South Africa, Bahrain, Spain, Mexico, Costa Rica, Romania..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1625-2020) 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 April 8, 2020. 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.