Clinical Resolution Laboratory Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
USClinical Resolution Laboratory Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
Recalling Firm: Clinical Resolution Laboratory, Inc. of Brea, Calif.
Grund für den Rückruf / Gefahr
TranslatedThe packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream contains lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.
Produktbeschreibung & Identifikation
TranslatedThis recall involves Numb 100 Topical Anesthetic Cream. The recalled cream is in a 1.35 fluid ounce white jar with a rounded cap. Numb 100 Topical Anesthetic Cream and a blue cross are printed on the jar's front panel.
Betroffene Produkte
TranslatedNumb 100 Topical Anesthetic Cream
Additional Source Details
| Field | Value |
|---|---|
| U R L | https://www.cpsc.gov/Recalls/2019/Clinical-Resolution-Laboratory-Recalls-Topical-Anesthetic-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirement-Risk-of-Poisoning |
| Title | Clinical Resolution Laboratory Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning |
| Images › U R L | https://www.cpsc.gov/s3fs-public/Recalled Numb 100 topical anesthetic cream.jpg |
| Images › Caption | Recalled Numb 100 topical anesthetic cream |
| Hazards › Name | The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream contains lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it. |
| Injuries › Name | None reported |
| Products › Name | Numb 100 Topical Anesthetic Cream |
| Products › Number Of Units | 26500 |
| Recall I D | 8500 |
| Remedies › Name | Consumers should immediately place the recalled topical anesthetic out of reach of children and contact Clinical Resolution Laboratory for a full refund, a free replacement cream, or free replacement child-resistant cap. |
| Retailers › Name | Laser Jet and other health and beauty stores nationwide and online at www.amazon.com and www.laserjetinc.com from May 2017 through November 2018 for about $18. |
| Recall Date | 2019-02-28T00:00:00 |
| Description | This recall involves Numb 100 Topical Anesthetic Cream. The recalled cream is in a 1.35 fluid ounce white jar with a rounded cap. Numb 100 Topical Anesthetic Cream and a blue cross are printed on the jar's front panel. |
| Distributors › Name | Laser Jet, Inc. of Brooklyn, N.Y. |
| Recall Number | 19076 |
| Manufacturers › Name | Clinical Resolution Laboratory, Inc. of Brea, Calif. |
| Remedy Options › 1 › Option | Refund |
| Remedy Options › 2 › Option | Replace |
| Consumer Contact | Clinical Resolution Laboratory toll-free at 877-566-9687 from 8 a.m. to 5 p.m. PT Monday to Friday, email at info@clinicalresolution.com or online at www.clinicalresolution.com and click on the Recall Information tab at the top of the page for more information. |
| Last Publish Date | 2019-02-28T00:00:00 |
| Manufacturer Countries › Country | United States |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsCheck the model number, serial number, and date stamp on the rating label on the back or underside of the product.
Immediately discontinue using the product. Unplug electrical items and keep juvenile items out of reach of children.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (CPSC).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought Clinical Resolution Laboratory Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement;...?
Immediately stop using the product and keep it out of reach of children. Disconnect power if electrical, and do not attempt makeshift home repairs.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (CPSC). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Übersicht
- Rückrufendes UnternehmenClinical Resolution Laboratory, Inc. of Brea, Calif.
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🚨 SAFETY ALERT: Clinical Resolution Laboratory, Inc. of Brea, Calif. - Clinical Resolution Laboratory Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning Check if your household is affected: https://therecallfile.com/de/recalls/clinical-resolution-laboratory-recalls-topical-anesthetic-due-to-failu/CPSC-19076
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