-
Recalled Geri-Care Brand Extra Strength Acetaminophen 500mg tablets 1,000-count bottle -
Recalled Geri-Care Brand Regular Strength Enteric Coated Aspirin 325mg tablets 250-count bottle -
Recalled Geri-Care Brand Regular Strength Enteric Coated Aspirin 325mg tablets 1,000-count bottle -
Recalled Geri-Care Brand Adult Low Dose Enteric Coated Aspirin 81mg tablets 300-count bottle -
Recalled Geri-Care Brand Adult Low Dose Enteric Coated Aspirin 81mg tablets 1,000-count bottle
The over-the-counter drug products contain regulated substances which must be in child resistant packaging 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.
About 800
Geri-Care Pharmaceuticals at 800-540-3765 from 9 a.m. to 5 p.m. ET Monday through Thursday and 9 a.m. to 1 p.m. ET Friday, email at recalls@gericarepharm.com, or online at www.gericarepharm.com/recalls/ or www.gericarepharm.com and click on “Product Recalls” at the top of the page for more information.
Recall Details
This recall involves bottles of Geri-Care Brand over-the-counter acetaminophen and aspirin. The acetaminophen is 500mg with 1,000 tablets in the bottle. The aspirin was sold in 81mg with 300 and 1,000 tablets in the bottle and 325mg with 250 and 1,000 tablets in the bottle.
|
Product |
Count |
|
Extra Strength Acetaminophen 500mg Tablets |
1,000 |
|
Regular Strength Enteric Coated Aspirin 325mg Tablets |
250 |
|
Regular Strength Enteric Coated Aspirin 325mg Tablets |
1,000 |
|
Adult Low Dose Enteric Coated Aspirin 81mg Tablets |
300 |
|
Adult Low Dose Enteric Coated Aspirin 81mg Tablets |
1,000 |
Consumers should immediately store the recalled products in a safe location out of sight and reach of children, and safely dispose of the recalled product as soon as is practicable. Contact Geri-Care Pharmaceuticals for a full refund or replacement over-the-counter drug product.
None reported
Note: Individual Commissioners may have statements related to this topic. Please visit www.cpsc.gov/commissioners to search for statements related to this or other topics.
Related Recalls
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The recalled baby nests violate the safety requirements of CPSC’s Safety Standard for Infant Sleep Products, posing a suffocation risk and fall and entrapment hazards to infants. The failures include not having a stand and not meeting the requirements for side height, sleeping pad thickness, and fabric-sided openings. The product’s sides are shorter than the minimum side height limit; the sleeping pad’s thickness exceeds the maximum limit; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped.
Additionally, the baby nest designs with head pillows violate the Safe Sleep for Babies Act of 2021’s ban on inclined sleepers for infants because their sleep surfaces are inclined greater than ten degrees. Infant fatalities have occurred in inclined sleepers, after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances.
Infants can suffocate if they roll or move on the crib bumper in a position that obstructs breathing. Padded crib bumpers are banned under the Safe Sleep for Babies Act of 2021.
The recalled children’s pajamas violate the flammability regulations for children’s sleepwear, posing a risk of burn injuries to children.
The U.S. Consumer Product Safety Commission (CPSC) is charged with protecting the public from unreasonable risk of injury or death associated with the use of thousands of types of consumer products. Deaths, injuries, and property damage from consumer product-related incidents cost the nation more than $1 trillion annually. CPSC's work to ensure the safety of consumer products has contributed to a decline in the rate of injuries associated with consumer products over the past 50 years.
Federal law prohibits any person from selling products subject to a Commission ordered recall or a voluntary recall undertaken in consultation with the CPSC.
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