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CPSC recall · Reported September 11, 2020

Medique Recalls 31 Different Over-the-Counter Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold Exclusively on Amazon.com (Recall Alert)

The over-the-counter products contain regulated substances which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packagi…

Recall #
20780
Affected scope
About 143,300
Verify with CPSC →
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Medique, of Fort Myers, Fla. recalled The recall involves 31 different over-the-counter drugs purchased on or after June 1, 201… - a moderate-severity action.

Medique Recalls 31 Different Over-the-Counter Drugs Due to Failure to Meet Child Resistan… was recalled by Medique, of Fort Myers, Fla. in September 11, 2020. Reason: The over-the-counter products contain regulated substances which must be in child resistant packaging when be…. Remedy: Consumers should immediately store the recalled products in a safe location out of reach …. Verify recall #20780 with the CPSC before acting.

The recall

Medique, of Fort Myers, Fla. issued this moderate-severity CPSC recall-The over-the-counter products contain regulated substances which must be in child resistant packaging when be….

Moderate
severity level
September 11, 2020
reported

Sourced from official CPSC enforcement records. Verify recall #20780 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This CPSC action (record #20780) was formally reported on September 11, 2020. It is classified under Moderate severity, with a current status of Active. Medique, of Fort Myers, Fla. is listed as the recalling firm. Federal records list the affected scope as About 143,300.

The documented reason for this recall is: The over-the-counter products contain regulated substances which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packaging Act (PPPA). The packaging of the prod… 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 store the recalled products in a safe location out of reach of children and contact Medique for information on how to dispose of the product and receive a full refund. Al… - 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 - 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.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,287 drugs & medications recalls on record

-50005001,0001,5002,000 2006201220152018202120242026 263
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

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.

Severity

Moderate

Affected scope

About 143,300

Related Recalls

6

0 from same agency

Product description

The recall involves 31 different over-the-counter drugs purchased on or after June 1, 2018 that are unexpired from the following brands: Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp, and Ecolab. They include aspirin-containing products, acetaminophen-containing products, ibuprofen-containing products, lidocaine-containing products, diphenhydramine, loperamide, and naproxen products. The expiration date for tablets and creams can be found on either the top or side panels of the container carton in the format [YEAR/MO]. For products in spray bottles, the expiration date in the same format is located on the front of the bottle. The expiration date is found on the bottom for the spray cans. The 31 different recalled products are listed in the table below: Product Drug Package Type # of Packets Medi-First Non-Aspirin Acetaminophen acetaminophen (325 mg) 2 tablets packet 50 250 Medi-First Extra Strength Non-Aspirin Acetaminophen acetaminophen (500 mg) 2 tablets packet 50 125 250 Medi-First Sinus Pain & Pressure acetaminophen (500 mg) 2 tablets packet 50 125 250 Medique APAP acetaminophen (325 mg) 2 tablets packet 250 Medique Extra Strength APAP acetaminophen (500 mg) 2 tablets packet 50 125 250 Medique Back Pain-Off acetaminophen (250 mg) 2 tablets packet 50 100 250 Medique CCP Caffeine Fee acetaminophen (325 mg) 2 tablets packet 50 250 Medi-First Cold Relief acetaminophen (325 mg) 2 tablets packet 50 125 250 Medique Cramp Tabs acetaminophen (325 mg) 2 tablets packet 50 125 250 Medique Decorel Forte Plus acetaminophen (325 mg) 2 tablets packet 50 250 Medique Medicidin-D acetaminophen (325 mg) 2 tablets packet 50 100 250 Dover Aminofen acetaminophen (325 mg) 2 tablets packet 250 Otis Clapp Back Quell acetaminophen (200 mg) 2 tablets packet 150 Otis Clapp Mygrex acetaminophen (500 mg) 2 tablets packet 150 Otis Clapp Valihist acetaminophen (325 mg) 2 tablets packet 150 Medi-First Pain Relief Extra Strength acetaminophen (110 mg) aspirin (162 mg) 2 tablets packet 50 100 250 Medi-First Plus Pain Zappers acetaminophen (250 mg) aspirin (250 mg) 2 tablets packet 50 125 Medique Pain-Off acetaminophen (250 mg) aspirin (250 mg) 2 tablets packet 50 100 250 Medi-First Aspirin aspirin (325 mg) 2 tablets packet 50 125 250 Medi-First Plus Aspirin aspirin (325 mg) 2 tablets packet 50 125 Medique Aspirin aspirin (325 mg) 2 tablets packet 12 100 250 Medique Diphen diphenhydramine (25 mg) 1 tablet packet 24 200 Medi-First Ibuprofen ibuprofen (200 mg) 2 tablets packet 4 50 125 250 Medique I-Prin ibuprofen (200 mg) 2 tablets packet 3 100 250 Dover Addaprin ibuprofen (200 mg) 2 tablets packet 250 Medi-First Burn Cream with Lidocaine lidocaine (0.9 grams) packets 25 Medi-First Burn Spray lidocaine HCl (2%) 2 oz bottle -- Medi-First Blood Clotting Spray lidocaine (4%) 3 oz bottle -- Ecolab Burn Cream lidocaine (0.9 grams) packets 25 Medique Diamode loperamide HCl (2 mg) 1 tablet packet 6 50 100 Medique Mediproxen naproxen sodium (220 mg) 1 tablet packet 50 100

Reason for recall

The over-the-counter products contain regulated substances which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

Remedy, what to do

Consumers should immediately store the recalled products in a safe location out of reach of children and contact Medique for information on how to dispose of the product and receive a full refund. All known purchasers are being notified directly.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 20780
Date reported September 11, 2020
Date initiated September 11, 2020
Recalling firm Medique, of Fort Myers, Fla.
Affected scope About 143,300
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 store the recalled products in a safe location out of reach of children and contact Medique for info…

  • Check the recall number (20780) 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?
The recall involves 31 different over-the-counter drugs purchased on or after June 1, 2018 that are unexpired from the following brands: Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp, and Ecolab. They include aspirin-containing products, acetaminophen-containing products, ibuprofen-containing products, lidocaine-containing products, diphenhydramine, loperamide, and naproxen products. The expiration date for tablets and creams can be found on either the top or side panels of the container carton in the format [YEAR/MO]. For products in spray bottles, the expiration date in the same format is located on the front of the bottle. The expiration date is found on the bottom for the spray cans. The 31 different recalled products are listed in the table below: Product Drug Package Type # of Packets Medi-First Non-Aspirin Acetaminophen acetaminophen (325 mg) 2 tablets packet 50 250 Medi-First Extra Strength Non-Aspirin Acetaminophen acetaminophen (500 mg) 2 tablets packet 50 125 250 Medi-First Sinus Pain & Pressure acetaminophen (500 mg) 2 tablets packet 50 125 250 Medique APAP acetaminophen (325 mg) 2 tablets packet 250 Medique Extra Strength APAP acetaminophen (500 mg) 2 tablets packet 50 125 250 Medique Back Pain-Off acetaminophen (250 mg) 2 tablets packet 50 100 250 Medique CCP Caffeine Fee acetaminophen (325 mg) 2 tablets packet 50 250 Medi-First Cold Relief acetaminophen (325 mg) 2 tablets packet 50 125 250 Medique Cramp Tabs acetaminophen (325 mg) 2 tablets packet 50 125 250 Medique Decorel Forte Plus acetaminophen (325 mg) 2 tablets packet 50 250 Medique Medicidin-D acetaminophen (325 mg) 2 tablets packet 50 100 250 Dover Aminofen acetaminophen (325 mg) 2 tablets packet 250 Otis Clapp Back Quell acetaminophen (200 mg) 2 tablets packet 150 Otis Clapp Mygrex acetaminophen (500 mg) 2 tablets packet 150 Otis Clapp Valihist acetaminophen (325 mg) 2 tablets packet 150 Medi-First Pain Relief Extra Strength acetaminophen (110 mg) aspirin (162 mg) 2 tablets packet 50 100 250 Medi-First Plus Pain Zappers acetaminophen (250 mg) aspirin (250 mg) 2 tablets packet 50 125 Medique Pain-Off acetaminophen (250 mg) aspirin (250 mg) 2 tablets packet 50 100 250 Medi-First Aspirin aspirin (325 mg) 2 tablets packet 50 125 250 Medi-First Plus Aspirin aspirin (325 mg) 2 tablets packet 50 125 Medique Aspirin aspirin (325 mg) 2 tablets packet 12 100 250 Medique Diphen diphenhydramine (25 mg) 1 tablet packet 24 200 Medi-First Ibuprofen ibuprofen (200 mg) 2 tablets packet 4 50 125 250 Medique I-Prin ibuprofen (200 mg) 2 tablets packet 3 100 250 Dover Addaprin ibuprofen (200 mg) 2 tablets packet 250 Medi-First Burn Cream with Lidocaine lidocaine (0.9 grams) packets 25 Medi-First Burn Spray lidocaine HCl (2%) 2 oz bottle -- Medi-First Blood Clotting Spray lidocaine (4%) 3 oz bottle -- Ecolab Burn Cream lidocaine (0.9 grams) packets 25 Medique Diamode loperamide HCl (2 mg) 1 tablet packet 6 50 100 Medique Mediproxen naproxen sodium (220 mg) 1 tablet packet 50 100. Recalled by Medique, of Fort Myers, Fla.. Units affected: About 143,300.
Why was this product recalled?
The over-the-counter products contain regulated substances which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
What should consumers do?
Consumers should immediately store the recalled products in a safe location out of reach of children and contact Medique for information on how to dispose of the product and receive a full refund. All known purchasers are being notified directly.
Which agency issued this recall?
This recall was issued by the CPSC on September 11, 2020. Severity: Moderate. Recall number: 20780.
How do I check if my product is affected by a recall?
Check the product description and recall number (20780) 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.

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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: CPSC, reported September 11, 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.