Disetronic Medical Systems Inc.Announces a recall of the ACCU-CHEK Spirit insulin pump due to "up" and/or "down" button failures (April 30)
Thu, 30 Apr 2009 14:14:00 -0500
The pumps in question have serial numbers in the range from SN02119552 through SN10006093 (US market).
| FOR IMMEDIATE RELEASE April 29, 2009 Release #09-202 | Firm's Recall Hotline: (888) 823-0343 |
Name of Product: Under Armour Athletic Cups
Units: About 211,000
Importer: Under Armour Inc, of Baltimore, Maryland
Hazard: The cups can break if hit, posing a risk of serious injury hazard to athletes.
Incidents/Injuries: Under Armour has received five reports of cups breaking, including an injury involving cuts and bruising.
Personal Care Products Conducts Nationwide Recall of Non-Acetone Nail Polish Remover Because of Possible Health Risk (April 29)
Wed, 29 Apr 2009 06:19:00 -0500
Personal Care Products of Bingham Farms, MI is voluntarily conducting a nationwide recall of all lots of Personal Care non-acetone nail polish remover, conditioner enriched with gelatin, 6 fl. oz., UPC 4815592076, because it does not meet product specifications and has the potential to cause chemical burns to the fingers of users.
Nature and Health Co. Issues Voluntary Nationwide Recall of Libimax, a Product Marketed as a Dietary Supplement (April 27)
Wed, 29 Apr 2009 12:57:00 -0500
The recalled Libimax is sold as a 1 capsule individual pack or 10-capsule and 20-capsule plastic bottles in retail stores in California, Georgia, Illinois, Texas, and Ohio. The product label neither states it contains tadalafil nor warns consumers with high blood pressure not to ingest the product.
Universal ABC Beauty Supply International, Inc. Issues a Voluntary Nationwide Recall of Dietary Supplement Products Found to Contain an Undeclared Drug Ingredient (April 20)
Wed, 22 Apr 2009 11:11:00 -0500
Universal ABC Beauty Supply International, Inc. has been informed by the Food and Drug Administration (FDA) that FDA lab analyses of the dietary supplements distributed by the company were found to contain undeclared Sibutramine, an FDA-approved drug used as an appetite suppressant for weight loss. These dietary supplements are not supposed to contain Sibutramine. The FDA has not approved these products, therefore the safety and effectiveness of these products is unknown.
Neilgen Pharma Inc. and Advent Pharmaceutical Recall All Prescription Cough and Cold Drug Products Sold on or after March 5, 2008 (April 20)
Tue, 21 Apr 2009 06:49:00 -0500
Neilgen Pharma Inc. of Westminster, MD and Advent Pharmaceutical of East Windsor, NJ are recalling all prescription cough and cold drug products sold on or after March 5, 2008. Neilgen Pharma and Advent Pharmaceutical are contract manufacturers for these products and are recalling the products due to the unapproved drug product category.
ION Labs Inc. Recalls Influend Cough and Cold Products, in Alabama, Because Of Possible Health Risk
Wed, 15 Apr 2009 12:05:00 -0500
ION Labs Inc. of Clearwater, FL. is voluntarily recalling all of the Influend Cough and Cold products sold on or after May 30, 2008. ION Labs Inc. is Recalling the listed products due to the products not tested in conformance with the specifications of the lab, therefore the products may have a possibility to be super potent. Possible complications may include Tachycardia, palpitations, arrhythmias, cardiovascular collapse with hypotension, headaches, dizziness, anxiety, restlessness and nervousness.
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