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CPSCGeneral Alert

Chase Laboratories And Geneva Generics Recall Prenatal Vitamins With Folic Acid Due To Potential Iron Toxicity Hazard

Published: March 10, 1992Recall ID: 92061Category: Consumer ProductsCountry: United States
US
Safety AlertCPSCUSUS

Chase Laboratories And Geneva Generics Recall Prenatal Vitamins With Folic Acid Due To Potential Iron Toxicity Hazard

Recalling Firm: Chase Laboratories, Geneva Generics

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Reason for Recall / Hazard

Poisoning

Product Description & Identification

March 10, 1992 Release # 92-061 Chase Laboratories And Geneva Generics Recall Prenatal Vitamins With Folic Acid Due To Potential Iron Toxicity Hazard PRODUCT: "Prenatal Vitamins with Folic Acid" by Chase Laboratories under the Geneva Generics label, containing 100 tablets of vitamins with iron. PROBLEM: Lack of child-resistant closure means that a child could accidentally swallow these vitamins with iron. Just four or five tablets if consumed by a child at one time can cause serious illness or death. WHAT TO DO: Immediately return the "Prenatal Vitamins with Folic Acid" (100-tablet bottles) to the store where purchased for a refund of the purchase price. WASHINGTON, DC - In cooperation with the U.S. Consumer Product Safety Commission (CPSC), Chase Laboratories, Inc. of Newark, NJ is voluntarily recalling their 100 tablet bottles of "Prenatal Vitamins with Folic Acid" packaged under the Geneva Generics label because they are not packaged with child-resistant closures. The product intended for pregnant or lactating women, contains 60 milligrams of iron per tablet. The iron contained in just four or five tablets, if consumed by a child at one time, can cause serious illness or death. The recalled Prenatal Vitamins contain 100 tablets with a total of 6,000 milligrams (mg) of iron. The package is not child-resistant as required by the Poison Prevention Packaging Act. The CPSC enforces the requirement that any over-the-counter medication or dietary supplement which contains more than 250 mg of iron in a single package must be supplied with child- resistant packaging. Chase Laboratories reported the packaging problem and their initiation of the recall to CPSC under the reporting requirements of Section 15(b) of the Consumer Product Safety Act, 15 U.S.C. {2064(b). Consumers should immediately return the product to the store where purchased for a refund of the purchase price. Since the product's introduction in 1990, approximately 70,000 bottles of Prenatal Vitamins with Folic Acid packaged under the Geneva Generics Label were distributed in non-child-resistant packaging through 342 retail and wholesale druggists nationwide. Chase Laboratories, the manufacturer, and Geneva Generics, the private label distributor, instituted the recall of this product because of the potential hazard to children from these tablets due to the lack of child- resistant packaging. Neither of the recalling firms nor the Commission is aware of any poisoning incidents due to this product. Data from the American Association of Poison Control Centers report that 11 children in the United States died in 1991 from ingestion of iron-containing medicines and dietary supplements. CPSC is announcing this recall as part of its mission to protect the public from unreasonable risks of injury and death associated with consumer products. The Commission's objective is to reduce the estimated 28.5 million injuries and 21,600 deaths associated each year with the 15,000 different types of consumer products under CPSC's jurisdiction

Affected Products

Geneva Generics Prenatal Vitamins with Folic Acid

Additional Source Details

FieldValue
U R Lhttps://www.cpsc.gov/Recalls/1992/Chase-Laboratories-And-Geneva-Generics-Recall-Prenatal-Vitamins-With-Folic-Acid-Due-To-Potential-Iron-Toxicity-Hazard-
TitleChase Laboratories And Geneva Generics Recall Prenatal Vitamins With Folic Acid Due To Potential Iron Toxicity Hazard
Hazards › NamePoisoning
Products › NameGeneva Generics Prenatal Vitamins with Folic Acid
Products › TypeVitamins & Supplements
Products › Category I D2222
Recall I D5251
Recall Date1992-03-10T00:00:00
DescriptionMarch 10, 1992 Release # 92-061 Chase Laboratories And Geneva Generics Recall Prenatal Vitamins With Folic Acid Due To Potential Iron Toxicity Hazard PRODUCT: "Prenatal Vitamins with Folic Acid" by Chase Laboratories under the Geneva Generics label, containing 100 tablets of vitamins with iron. PROBLEM: Lack of child-resistant closure means that a child could accidentally swallow these vitamins with iron. Just four or five tablets if consumed by a child at one time can cause serious illness or death. WHAT TO DO: Immediately return the "Prenatal Vitamins with Folic Acid" (100-tablet bottles) to the store where purchased for a refund of the purchase price. WASHINGTON, DC - In cooperation with the U.S. Consumer Product Safety Commission (CPSC), Chase Laboratories, Inc. of Newark, NJ is voluntarily recalling their 100 tablet bottles of "Prenatal Vitamins with Folic Acid" packaged under the Geneva Generics label because they are not packaged with child-resistant closures. The product intended for pregnant or lactating women, contains 60 milligrams of iron per tablet. The iron contained in just four or five tablets, if consumed by a child at one time, can cause serious illness or death. The recalled Prenatal Vitamins contain 100 tablets with a total of 6,000 milligrams (mg) of iron. The package is not child-resistant as required by the Poison Prevention Packaging Act. The CPSC enforces the requirement that any over-the-counter medication or dietary supplement which contains more than 250 mg of iron in a single package must be supplied with child- resistant packaging. Chase Laboratories reported the packaging problem and their initiation of the recall to CPSC under the reporting requirements of Section 15(b) of the Consumer Product Safety Act, 15 U.S.C. {2064(b). Consumers should immediately return the product to the store where purchased for a refund of the purchase price. Since the product's introduction in 1990, approximately 70,000 bottles of Prenatal Vitamins with Folic Acid packaged under the Geneva Generics Label were distributed in non-child-resistant packaging through 342 retail and wholesale druggists nationwide. Chase Laboratories, the manufacturer, and Geneva Generics, the private label distributor, instituted the recall of this product because of the potential hazard to children from these tablets due to the lack of child- resistant packaging. Neither of the recalling firms nor the Commission is aware of any poisoning incidents due to this product. Data from the American Association of Poison Control Centers report that 11 children in the United States died in 1991 from ingestion of iron-containing medicines and dietary supplements. CPSC is announcing this recall as part of its mission to protect the public from unreasonable risks of injury and death associated with consumer products. The Commission's objective is to reduce the estimated 28.5 million injuries and 21,600 deaths associated each year with the 15,000 different types of consumer products under CPSC's jurisdiction
Recall Number92061
Manufacturers › 1 › NameChase Laboratories
Manufacturers › 2 › NameGeneva Generics
Last Publish Date2015-01-22T00:00:00

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Check the model number, serial number, and date stamp on the rating label on the back or underside of the product.

2Isolate & Discontinue Use

Immediately discontinue using the product. Unplug electrical items and keep juvenile items out of reach of children.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

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 Guide

Q1:What should I do immediately if I own or bought Chase Laboratories And Geneva Generics Recall Prenatal Vitamins With Folic Acid Due To Potential Iron Toxicity Hazard?

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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Overview

  • Recalling FirmChase Laboratories, Geneva Generics
Recall Hazard Severity
Caution (Class III)
Official Agency Alert

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