Severity
Moderate
ModerateActive
CPSC recall · Reported October 1, 2018
UberScientific Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream and spray contain lidocaine, posing a risk of poisoning to young …
UberScientific LLC, of Kissimmee, Fla. recalled This recall involves UberScientific Uber Numb Topical Anesthetic Cream and Uber Numb Spra… - a moderate-severity action.
UberScientific Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure … was recalled by UberScientific LLC, of Kissimmee, Fla. in October 1, 2018. Reason: The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving c…. Remedy: Consumers should immediately place the recalled topical anesthetic out of reach of childr…. Verify recall #19001 with the CPSC before acting.
The recall
UberScientific LLC, of Kissimmee, Fla. issued this moderate-severity CPSC recall-The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving c….
- Moderate
- severity level
- October 1, 2018
- reported
Sourced from official CPSC enforcement records. Verify recall #19001 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #19001) was formally reported on October 1, 2018. It is classified under Moderate severity, with a current status of Active. UberScientific LLC, of Kissimmee, Fla. is listed as the recalling firm. Federal records list the affected scope as About 76,000.
The documented reason for this recall is: The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream and spray contain lidocaine, posing a risk of poisoning to young children if they put it on their skin or… Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately place the recalled topical anesthetic out of reach of children and contact UberScientific for instructions on how to receive a free replacement or full refund. Consumers … - consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls, 6 from CPSC - 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products 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
About 76,000
Related Recalls
6
6 from same agency
Product description
This recall involves UberScientific Uber Numb Topical Anesthetic Cream and Uber Numb Spray. The recalled cream is in a white jar with a smooth, rounded cap and a green label with "Uber Numb Topical Anesthetic Cream" printed on the front. The cream was sold in one, two and four ounce sizes with the lot numbers printed on the bottom of the jar and the UPC number printed on the label to the left of the product name. The brand name UberScientific is printed on the label below the net weight. The recalled spray is in a green bottle with a white cap and has a white label with "Uber Numb Spray" printed on the front. The spray was sold in four ounce size with the lot numbers printed on the bottom of the bottle and the UPC number printed on the label to the right of the product name. The brand name UberScientific is printed on the label to the left of the product name. Product Size UPC Lot Numbers UberScientific Uber Numb Topical Anesthetic Cream 1 oz. 00863255000306 A23Z3 and F12Z5 2 oz. 00863255000344 L06Z2A, L06Z2B, and B01N2A 4 oz. 0083255000313 E10Z4, L06Z2, and B01N2 Uber Numb Spray 4 oz. 00850777008002 K30Z6 and B09N2
Reason for recall
The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream and spray contain lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.
Remedy, what to do
Consumers should immediately place the recalled topical anesthetic out of reach of children and contact UberScientific for instructions on how to receive a free replacement or full refund. Consumers with the recalled cream can receive a free replacement cap that is child-resistant. Consumers with the recalled spray can receive a free replacement cream with the new child-resistant cap or a full refund.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 19001 |
| Date reported | October 1, 2018 |
| Date initiated | October 1, 2018 |
| Recalling firm | UberScientific LLC, of Kissimmee, Fla. |
| Affected scope | About 76,000 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately place the recalled topical anesthetic out of reach of children and contact UberScientific for instru…
- Check the recall number (19001) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC 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? ▼
This recall involves UberScientific Uber Numb Topical Anesthetic Cream and Uber Numb Spray. The recalled cream is in a white jar with a smooth, rounded cap and a green label with "Uber Numb Topical Anesthetic Cream" printed on the front. The cream was sold in one, two and four ounce sizes with the lot numbers printed on the bottom of the jar and the UPC number printed on the label to the left of the product name. The brand name UberScientific is printed on the label below the net weight. The recalled spray is in a green bottle with a white cap and has a white label with "Uber Numb Spray" printed on the front. The spray was sold in four ounce size with the lot numbers printed on the bottom of the bottle and the UPC number printed on the label to the right of the product name. The brand name UberScientific is printed on the label to the left of the product name. Product Size UPC Lot Numbers UberScientific Uber Numb Topical Anesthetic Cream 1 oz. 00863255000306 A23Z3 and F12Z5 2 oz. 00863255000344 L06Z2A, L06Z2B, and B01N2A 4 oz. 0083255000313 E10Z4, L06Z2, and B01N2 Uber Numb Spray 4 oz. 00850777008002 K30Z6 and B09N2. Recalled by UberScientific LLC, of Kissimmee, Fla.. Units affected: About 76,000.
Why was this product recalled? ▼
The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream and spray contain lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.
What should consumers do? ▼
Consumers should immediately place the recalled topical anesthetic out of reach of children and contact UberScientific for instructions on how to receive a free replacement or full refund. Consumers with the recalled cream can receive a free replacement cap that is child-resistant. Consumers with the recalled spray can receive a free replacement cream with the new child-resistant cap or a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on October 1, 2018. Severity: Moderate. Recall number: 19001.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (19001) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
CPSC Moderate
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Compare this recall with AMASKY Nursing Pillows Recalled Due to Risk of Serious Inju… →
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: CPSC, reported October 1, 2018. 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.