Product Recalls

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January 21, 2019
Cardinal Health Curity All Purpose Sponges

Product does not meet sterilization requirements.

Remedy:
Inspect your inventory for affected product code and lot number (18E190262)

Units:
About 1

CONTACT INFORMATION:

Download:
Product Recall Details

October 10, 2018
Valeant Pharmaceutic has voluntarily issued a recall on Ocean Saline Nasal Spray due to a possible microbial contamination.

A microbial contamination, Pseudomonas aeruginosa, is the possible exposure of a product to micro-organisms, such as fungi, bacteria, viruses and their biological by-product, which may cause disease and allergic responses to occupants.

Remedy:
Customers should check the UPC’s Ocean branded products in their homes to be sure none of the affected product has been purchased.

CONTACT INFORMATION:

Email:
Valeant8985@Stericycle.com

Phone:
(888) 667-1502

Download:
Product Recall Details

October 1, 2018
B.Braun Rate Flow Regulator Administration Sets

B. Braun Medical Inc. (BBMI) is issuing a voluntary medical device recall of Rate Flow® Regulator Administration sets due to reported deficiencies in the manufacturer's quality systems at its manufacturing facility. Rate Flow Regulator Administration sets are manufactured by Leventon S.A.U. and purchased as a finished product by BBMI.

Remedy:
Contact Braun for next steps for product removal.

CONTACT INFORMATION:

Website:
http://www.fda.gov/medwatch/report.htm

Email:
PA_QualityAssurance.BBMUS_Service@bbraunusa.com

Phone:
(610) 266-0500

Download:
Product Recall Details

September 10, 2018
CoaguChek XS PT Test strips used with all Professional and Patient Self-Testing instruments.

Roche Diagnostics has calibrated CoaguChek XS PT test strips to the latest World Health Organization International Reference Preparation (rTF/16). The previous International Reference Preparation (IRP) was rTF/09. Since this calibration, Roche Diagnostics has been informed by some customers of abnormally high INR test results.

Remedy:
Please contact Roche Diagnostics Point-of-Care Trachinacl Service, 24 hours a day, seven days a week.

Units:
About 625,000

CONTACT INFORMATION:

Website:
http://www.coaguchek-usa.com

Phone:
(800) 428-4674

Download:
Product Recall Details

May 22, 2018
Medline Industries, Inc. is recalling specific lots of ReadyFlush Wipes with 3.2% Dimethicone.

Immediately check your stock for item number MSC263811 and the affected lot numbers, 18BE0005 & 18BE0006, quarantine all affected product.

Remedy:
Please call/email us for a response form listing the quantity of affected product on hand.

CONTACT INFORMATION:

Website:
http://www.medline.com

Email:
Recalls@Medline.com

Phone:
(866) 359-1704

Download:
Product Recall Details

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