Wood And Metal In Rolaids Activates The Recall Of Its 13 Million Packages
December 10th, 2010 - 8:27 pm ICT by Pen Men At WorkDecember 10, 2010 (Pen Men at Work): McNeil Consumer Healthcare (MCH), which is a division under the famous pharmaceutical company, Johnson & Johnson (J&J), has asserted that it is going to recall innumerable packages, numbering millions, of Rolaids, which represent the frequently utilized antacid. JJ has reportedly attained numberless grievances about the Rolaids, which consist of complaints such as the presence of foreign particles such as wood and metal in the product. The New York Times (NYT) has articulated that 13 million packages of the over-the-counter pill will be a part of the massive recall.
The MCH has asserted that its scrutiny has ascertained that the alien materials were possibly introduced into Rolaids during the manufacturing procedure at a third party manufacturer. However, MCH has endeavored to soothe the hassled consumers by uttering that the possibility of illnesses or injuries due to the usage of Rolaids is remote. It has urged the consumers to discontinue utilizing Rolaids as quickly as possible. Incorporated in the recall are Rolaids Extra Strength Softchews along with Rolaids Extra Strength plus Gas Softchews. Another product recalled is Rolaids Multi-Symptom plus Anti-Gas Softchews. Customers, who are fretful, can telephone McNeil at 1-888-222-6036, with the company then supplying directives about reimbursement.
On November 23, McNeil proclaimed that it was recalling 71,000 parcels of a cherry-flavored, extra-strength edition of Rolaids subsequent to consumer criticisms of an unusual consistency that was connected to crystallized sugar. In December, it also recalled 12 million bottles of its extensively employed over-the-counter heartburn medication, Mylanta, subsequent to leaving out tiny amounts of alcohol from the product’s sticker.
Edolphus Towns, the chairperson of the Government Oversight Committee of the American House, has uttered that the latest recall bequeaths a discomforting indication that the company continues to suffer from grave deficiencies vis-à-vis its quality control processes. The American Department of Justice as well as the Food and Drug Administration (FDA) are analyzing whether to initiate criminal charges against J& J or inflict civil penalties.
- Rolaids Recall Issued By Johnson & Johnson - Dec 10, 2010
- Johnson & Johnson announce recall for Fastmelt Tablets, Motrin Capsules & Rolaids softchews - Nov 24, 2010
- Tylenol Recall Expanded By Johnson & Johnson - Jul 09, 2010
- Johnson & Johnson Expands Recall Of Tylenol, Benadryl And Motrin - Jul 09, 2010
- Tylenol Arthritis Pain Caplet is being recalled - Jan 03, 2010
- FDA says that J&J knew about problems with Motrin long ago - May 28, 2010
- Rolaids' antacid recall is in place because of the presence of metal & wood particles in them - Dec 10, 2010
- Tylenol issues its first recall of 2010 - Jan 16, 2010
- Johnson & Johnson: Tylenol recall expanded - Jul 09, 2010
- McNeil Recall Of Tylenol After Reported Side Effects Leads To FDA Probe - May 26, 2010
- Congressional panel to investigate Tylenol's recall - May 07, 2010
- Tylenol Recall: Grave Side Effects Of Tylenol Being Examined By The FDA - May 26, 2010
- The CEO of Johnson & Johnson To Address Recalls - Sep 30, 2010
- Tylenol's 775 side effects being investigated - May 26, 2010
- Johnson & Johnson Knew Of Motrin Problems, Testified Before Lawmakers - May 28, 2010
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