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NJLINCS Health Alert Network

Public Health Info

Distributed by the New Jersey Department of Health

Subject: Food Recall

Empire Kosher Poultry, Inc., a Mifflintown, Pa. establishment, is recalling approximately 10,839 pounds of raw poultry products that may be contaminated with extraneous materials, specifically metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced.

The raw chicken breast products were produced and packaged on Nov. 2, 2017. The following products are subject to recall:

.4 to5.25-lbs. tray packages containing chicken breasts labeled “Empire KOSHER NATURAL Chicken Breasts, Boneless & Skinless” with case code 46375 and “Sell By” date 11/14/17.
.1 to1.25-lbs. tray packages containing chicken breasts labeled “Empire KOSHER NATURAL Chicken Breasts, Boneless & Skinless” with case code 7488 and “Sell By” date 11/16/17.
.2.5-lbs. tray packages containing chicken breasts labeled “Empire KOSHER NATURAL Chicken Breasts, Boneless & Skinless” with case code 7598 and “Sell By” date11/16/17.
.1 to1.25-lbs. tray packages containing chicken breasts labeled “Empire KOSHER NATURAL Chicken Breasts, Boneless & Skinless” with case code 92615 and “Sell By” date 11/17/17.
.1 to 1.25 -lbs. tray packages containing chicken breasts labeled “Empire KOSHER NATURAL Chicken Breasts, Boneless & Skinless” with case code 7888 and “Sell By” date 11/16/17.

The products subject to recall bear establishment number “P-1015” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

The problem was discovered on November 2, 2017 by an establishment employee who observed metal foreign material in a chicken breast while performing routine duties. The establishment took corrective actions to recover products before reaching commerce.

There have been no confirmed reports of adverse reactions due to consumption of these products. FSIS has received no reports of injury or illness from consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers with questions about the recall can contact the Empire Kosher toll free line at (800) 570-5718. Media with questions about the recall can contact MediaRelations@Hain.com.

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For all recalls – http://www.recalls.gov/recent.html

8-17-2017            Recall of Wholesale and Retail liquid products and liquid vitamin supplements manufactured by PharmaTech

Distribution firms: Leader Brand, Major Pharmaceuticals and Rugby Laboratories, have jointly issued a precautionary nationwide recall on August 3^rd, 2017 of all lots of liquid products manufactured by PharmaTech LLC, of Davis, Fl. Due to possible product contamination of Burkholderia cepacia (B. cepacia).  People who may have a weakened or developing immune systems or chronic lung disease like cystic fibrosis are most susceptible to bacterial infection that is often resistant to common antibiotics (CDC, 2016). High risk populations include infants, children, and the elderly, who may be more likely to use liquid products.  

Products subject to recall were distributed by Leader Brand, Major Pharmaceuticals, and Rugby Laboratories to both wholesale and retail facilities, including hospitals and pharmacies. Consumers, pharmacies, and healthcare facilities that have products which include but are not limited to, Diocto Syrup and Dioctor Liquid, should stop using and dispensing product immediately.

Consumers with questions regarding this recall should contact Rugby Laboratories/ Major Pharmaceuticals Customer Support at 1-800-645-2158, Monday through Friday 8 a.m- 8 p.m EST. Or Leader Customer Support at 1-800-200-6313 option #1, Monday through Thursday 8 a.m – 7 p.m and Friday 8 a.m – 5 p.m EST. Consumers can contact their physician or healthcare provider if they have additional questions about this product.

Adverse reactions or quality problems experienced with the use of these products may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax:

• Complete and submit the report Online: fda.gov/medwatch/report.htm
• Regular Mail or Fax: Download form fda.gov/MedWatch/getforms.htmor call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

Please see the below list of affected products: