Metal
All Recalls
95,102 total recalls in our database
Use of ingredient with violative pesticide residue.
Metal
Curry Chicken Salad Rollup, 7oz UPC 265325
Whole Foods Market Group
Product contaminated with Listeria monocytogenes
Use of ingredient with violative pesticide residue.
Metro Irresistibles Gluten Free Cheese Ravioli 6- 9 ounce bags Use By 020317; Imported for Metro Brands, Montreal Quebec, H1C 1V6, Toronto (Ontario) M9B 1B9 UPC 059749935609
Contes Pasta Company
This recall has been initiated due to possible contamination with Salmonella which was found in a raw product by a third party laboratory.
219773 509997 MARKET DISTRICT POPPYSEED LOG
Giant Eagle
All lots of Market District brand Apricot Logs and Poppyseed Logs prepared and sold individually from the Bakery department inside Giant Eagle and Market District supermarkets with sell by dates from November 7, 2015 through November 17, 2015 have been voluntarily recalled by Giant Eagle due to an undeclared milk allergen
Use of ingredient with violative pesticide residue.
Honey Mustard Mix sold under the following brand: Ashdon Farms, Net Wt. 8 oz. (227 g), UPC 79113-41184
A. L. Schutzman Company
The honey mustard mix lists whey in the ingredient list but does not list Milk in the Contains statement.
Curry Chicken Salad Wrap, Made Right Here, sold by weight, 12oz UPC 263144 UPC Code : 285551
Whole Foods Market Group
Product contaminated with Listeria monocytogenes
Irbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg, 90-count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICAL INDUSTRIES LTD Jerusalem, 971010 Israel, Manufactured for: TEVA PHARMACEUTICAL INDUSTRIES USA Sellersville, PA 18960. NDC 0093-8238-98
Teva Pharmaceutical Industries
Labeling: Incorrect or Missing Lot AND/OR Exp Date.
Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle
Myco Medical Supplies
Particulates: Complaints of rubber coring from the closure of injection vials.
MYLAΒΏ software connected to a Laboratory Information System (LIS) and a VITEKΒΏ 2 system has the potential to link a test result to an incorrect patient record with the same specimen ID.
Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version 3.0.2.0 and DxH 600 software version 1.1.1.0 because the software for the DxH systems allows the creation of multiple orders with the same Specimen identification (ID) but different Patient identification when manually editing pending orders at the System Manager.
Antibiotic concentration may be insufficient which may result in incorrect test results.
Philips Healthcare Ingenuity Core Computed Tomography X-ray system
Philips Electronics North America
During scans with specific protocol steps, the software unexpectedly sets the Axial ( 2 axis ) scan length to a different length than the user set in the plan.
Pod's needle mechanism fails to deploy or there is a delay in the deployment of the needle mechanism.
GE Healthcare has recently become aware of a potential safety issue related to a non-recoverable loss of displayed imaging (loss of monitor video) involving Optima CL323i & Optima IGS 320 systems.
MYLAΒΏ software connected to a Laboratory Information System (LIS) and a VITEKΒΏ 2 system has the potential to link a test result to an incorrect patient record with the same specimen ID.
Certain models and serial numbers of GlideScope GVL and AVL laryngoscope blades may separate, due to inadequate bonding of the silicone adhesive affixing the halves of the blade. The potential for blade separation may not be readily visible during routine inspection before or after intubation.