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Ready Pac, Trader Joe's Bagged Romaine Recalled For E. coli

RECALLTJoesAmericanRomaine lettuce and contact lenses have been recalled for health reasons; the romaine recall includes produce sold at several local stores. Read details about the lens recall below.

Ready Pac Foods, Inc. of Irwindale is recalling a total of 5,379 cases of  bagged salad products containing Romaine lettuce, as listed below, with the Use-by Date of November 18, 2011 because they may be contaminated with E. coli (E.coli O157:H7).

E.coli O157:H7 is an organism that may cause diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death.

The recall extends only to the listed products with this Use-by Date and sold in the following states: Arizona, California, Colorado, Hawaii, Idaho, Oregon, Texas, and Washington.  No other Ready Pac Foods, Inc. products are included in the recall.

PRODUCT DESCRIPTION

UPC #

BEST IF USED BY

10oz. Ready Pac Caesar Romaine

0-77745-00202-6

NOV 18

9.25oz Ready Pac Santa Fe Caesar Complete Salad

0-77745-21404-7

NOV 18

10oz. Ready Pac Classic Caesar Complete Salad

0-77745-20566-3

NOV 18

10oz. Ready Pac Bella Romaine

0-77745-21407-8

NOV 18

10oz. Dining In Classic Caesar Salad Kit

0-11225-02530-3

NOV 18

10oz. Raley’s Caesar Romaine

0-46567-71642-8

NOV 18

10oz. Trader Joe’s Romaine Salad

0013-2145

NOV 18

16oz. Trader Joe’s Very American Salad

0020-7225

NOV 18

10oz. Safeway Farms Caesar Romaine

0-21130-98350-6

NOV 18

9oz. Safeway Farms Hearts of Romaine

0-21130-98358-2

NOV 18

10oz. Safeway Farms Complete Caesar Supreme

0-21130-33677-7

NOV 18

10.25oz Safeway Farms Complete Southwestern Ranch

0-21130-33679-1

NOV 18

No illnesses related to these products have been reported.

The voluntary recall was initiated based on a single positive random sample result for E.coli O157:H7 reported to Ready Pac by the FDA. Ready Pac is fully cooperating with the FDA on the recall.

Because it is still possible that products bearing the Use-by Date of November 18, 2011 could be on store shelves, this recall extends to retailers as well as consumers. Ready Pac believes that it is important to alert consumers and retailers who might still possess one of the potentially affected salads to dispose of it immediately.

Instructions for Consumers:

Check your refrigerator for the above listed products with the Use-by Date of November 18, 2011. The Use-by Date can be found in the upper left hand corner of the package with the UPC numbers located on the back side of the bag.

Consumers who may have purchased the affected product are asked to record the Use-by Date and UPC number, immediately dispose of the product, and contact the Ready Pac Consumer Affairs representative, toll-free at (800) 800-7822, Monday – Friday, 8 a.m. to 5 p.m. (Pacific Time) to obtain a full refund.

Ready Pac Foods, Inc. has earned an outstanding safety record for over 40 years and has taken immediate precautionary measures to protect public health by issuing this voluntary recall and removing product from the market.  We have notified all of our retail customers who have received the product in question and directed them to remove it from their shelves.

CONTACT LENS RECALL

CooperVision announced today that it is expanding its worldwide recall of the Avaira brand product line of contact lenses to include a limited number of lots of Avaira Sphere contact lenses. In continued collaboration with the United States Food and Drug Administration, CooperVision is expanding the recall because it identified certain lots of Avaira Sphere lenses that did not meet its updated quality requirements due to the level of a silicone oil residue.

The presence of the residue (silicone oil) on Avaira Sphere contact lenses may cause hazy vision or discomfort, severe eye pain or eye injuries requiring medical treatment. Not everyone experiences the same symptoms.

“The company is confident we found the problem and have taken corrective action to fix the problem,” said Christine Moench, Vice President, Global Regulatory Affairs and Quality Assurance. “The health and safety of our customers is our top priority. ”

If you wear Avaira Sphere contact lenses and experience any symptoms, CooperVision recommends that you stop wearing the lenses immediately. Contact your eye care practitioner for advice.

Avaira Sphere contact lens wearers should:

CooperVision will launch a recall site www.coopervision.com/international-recall on Wednesday November 16th for wearers to enter the package lot number found on the contact lens carton or blister label to determine if their lenses have been recalled.

Alternatively, contact CooperVision on a toll-free consumer hotline at 1-855-526-6737(hours of operation 9:00am-5:00pm EST Monday-Friday)

If you discover your lenses are among the recalled lots, return them to the point of purchase or to your eye care practitioner.

Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Online at www.fda.gov/MedWatch/report.htm

Regular Mail; use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm

Fax 1 – 800 – FDA – 0178.

In August 2011, CooperVision announced a recall of limited lots of Avaira Toric contact lenses. CooperVision has identified the issue and has corrected it through its quality system process.

CooperVision will continue to supply Avaira Sphere lenses that are not affected by this recall.

As part of the expanded recall, CooperVision is notifying its customers and requests that eye care practitioners contact their patients regarding this recall. Communication efforts are focused at eye care professional and distributors to effectively reach lens wearers. CooperVision recall efforts include:

Sending worldwide recall notifications to Avaira Sphere CooperVision customers.

Issuing a press release via PR Newswire and Globe Newswire regarding the recall of limited lots of CooperVision Avaira Sphere lenses.

Providing information on the CooperVision website for lens wearers to check if their lenses are impacted (www.coopervision.com/international - recall).

An information notice has been posted on www.coopervision.com.

Offering a toll-free consumer hotline (1-855-526-6737 hours of operation 9:00-5:00pm EST Monday-Friday).

Providing retailers and distributors access to patient communications materials.

Providing support and detailed information to eye care practitioners to remove recalled lots of Avaira Sphere lenses from the market place.

Offering customer care resources to answer questions from patients.

The total number of Avaira Sphere lenses manufactured that are affected by the recall is 6.6M, of which 4.9M were shipped to customers globally. CooperVision intends to replace the recalled product with available Avaira Sphere inventory from lots that are not impacted by this recall action.

About CooperVision
CooperVision, a unit of The Cooper Companies, Inc. (NYSE: COO), is one of the world's leading manufacturers of soft contact lenses. The Company produces a full array of monthly, two-week and daily disposable contact lenses, all featuring advanced materials and optics. CooperVision has a strong heritage of solving the toughest vision challenges; such as astigmatism, presbyopia and ocular dryness; and offers the most complete collection of spherical, toric and multifocal products available. Through a combination of innovative products and focused practitioner support, the company brings a refreshing perspective to the marketplace, thereby creating real advantages for customers and wearers. For more information, visit www.coopervision.com.