Severity
Critical
CriticalClass ITerminated
FDA Devices recall · Reported August 20, 2014
Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe with hyaluronic acid concentration of 20 mg/ml. Product Usage: Expression is labelled as an Intranasal Splint, intended to minimize bleeding and edema and to prevent adhesions between the septum and the nasal cavity. However, Expression is currently being used off-label as a subcutaneously injected dermal filler.
Manufacturer made a change in the production process that resulted in a change in final gel weight. RECALL EXPANDED 7/8/2014 Firm expanded their recall to include all lots of …
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Enhancement Medical, LLC recalled Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe with hyal… - a critical-severity action.
Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe with hyal… was recalled by Enhancement Medical, LLC in August 20, 2014. Reason: Manufacturer made a change in the production process that resulted in a change in final gel weight. RECALL …. Check the official notice for the remedy. Verify recall #Z-2135-2014 with the FDA Devices before acting.
The recall
Enhancement Medical, LLC issued this critical-severity FDA Devices recall-Manufacturer made a change in the production process that resulted in a change in final gel weight. RECALL ….
- Critical
- severity level
- 18K units
- affected scope
- Class I
- classification
- August 20, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2135-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2135-2014) was formally reported on August 20, 2014, with the manufacturer initiating the action on August 7, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Enhancement Medical, LLC is listed as the recalling firm, operating out of Wauwatosa, WI. Federal records list the affected scope as 17,875.
The documented reason for this recall is: Manufacturer made a change in the production process that resulted in a change in final gel weight. RECALL EXPANDED 7/8/2014 Firm expanded their recall to include all lots of product. Distribution data in the federal record shows the product reached: Worldwide Distribution - USA (nationwide including Puerto Rico) and Internationally to Canada.. 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
17,875
Related Recalls
6
3 from same agency
Product description
Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe with hyaluronic acid concentration of 20 mg/ml. Product Usage: Expression is labelled as an Intranasal Splint, intended to minimize bleeding and edema and to prevent adhesions between the septum and the nasal cavity. However, Expression is currently being used off-label as a subcutaneously injected dermal filler.
Reason for recall
Manufacturer made a change in the production process that resulted in a change in final gel weight. RECALL EXPANDED 7/8/2014 Firm expanded their recall to include all lots of product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | Z-2135-2014 |
| Date reported | August 20, 2014 |
| Date initiated | August 7, 2013 |
| Recalling firm | Enhancement Medical, LLC |
| Firm location | Wauwatosa, WI |
| Affected scope | 17,875 |
| Distribution | Worldwide Distribution - USA (nationwide including Puerto Rico) and Internationally to Canada. |
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-2135-2014) 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? ▼
Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe with hyaluronic acid concentration of 20 mg/ml. Product Usage: Expression is labelled as an Intranasal Splint, intended to minimize bleeding and edema and to prevent adhesions between the septum and the nasal cavity. However, Expression is currently being used off-label as a subcutaneously injected dermal filler.. Recalled by Enhancement Medical, LLC. Units affected: 17,875.
Why was this product recalled? ▼
Manufacturer made a change in the production process that resulted in a change in final gel weight. RECALL EXPANDED 7/8/2014 Firm expanded their recall to include all lots of product.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 20, 2014. Severity: Critical. Recall number: Z-2135-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - USA (nationwide including Puerto Rico) and Internationally to Canada..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2135-2014) 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 20, 2014. 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.