🍎 Food Class I - Dangerous
The firm was notified that the product may contain peanuts.
All Recalls
92,900 total recalls in our database
GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle, UPC: 689466706222.
Genetic Edge Compounds
🍎 Food Class I - Dangerous
Product contains DMAA and Methylsynephrine.
Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., 6/case, packed in a stand-up pouch.
Meijer, Inc #816 - Grand River Packaging
🍎 Food Class I - Dangerous
The firm initiated a voluntary recall of Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., packed in a stand up pouch, due to mislabeling. The label declared cream, milk, and eggs, which were not part of the original formula. The label lacked the following ingredients: Spices, Artificial Flavors, Garlic Powder, Onion Powder, Dextrose, Worcestershire Sauce, Corn Syrup, Salt, Carmel Color, Sugar, Tamarind, Natural Flavor, Malic Acid, Olive Oil, Molasses Sucralose, Bourbon Whiskey, Sulfites & Celery Seeds.
🍎 Food Class I - Dangerous
Product may contain undeclared egg,
Blue Diamond Almonds Blanc DCD FN C (blanched diced fine); NET WT 11.34 Kg, 25 lbs. corrugated carton with poly liner; Product of the USA. Blue Diamond Almonds, Sacramento, CA
Blue Diamond Growers
🍎 Food Class I - Dangerous
Firm was notified by customer of a positive Salmonella result obtained when testing of the product on receipt.
💊 Drugs Class I - Dangerous
Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
💊 Drugs Class I - Dangerous
Presence of foreign substance: glass particle
Packaging breach may compromise sterility
🏥 Medical Devices Class I - Dangerous
Firm has identified that ARCHITECT SHBG results generated with the Potassium EDTA specimen tube type may demonstrate a negative shift relative to results generated with serum. There is a potential for falsely decreased ARCHITECT SHBG results to be generated when using the ARCHITECT SHBG assay with the Potassium EDTA specimen tube type.
DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
DePuy Mitek, Inc., a Johnson & Johnson
🏥 Medical Devices Class I - Dangerous
Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw
DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
DePuy Mitek, Inc., a Johnson & Johnson
🏥 Medical Devices Class I - Dangerous
Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw
Merge OrthoPACS software.
Merge Healthcare
🏥 Medical Devices Class I - Dangerous
A migrated study that has annotations will display the annotations, but when a prior study is loaded that should have annotations, the second study will not display annotations.
Dimension Vista Thyroid Stimulating Hormone (TSH) Flex reagent cartridge
Siemens Healthcare Diagnostics
🏥 Medical Devices Class I - Dangerous
The concentrations for Biotin listed in the Non-Interfering Substances section of the current Dimension and Dimension Vistat Instructions for Use (IFU) for Dimension TNI, Dimension Vista DIGXN, E2, FERR, PRL, and TSH have incorrect units, and incorrectly state the level at which biotin does not interfere.
DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
DePuy Mitek, Inc., a Johnson & Johnson
🏥 Medical Devices Class I - Dangerous
Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw
🏥 Medical Devices Class I - Dangerous
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
🏥 Medical Devices Class I - Dangerous
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
🏥 Medical Devices Class I - Dangerous
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
DePuy Mitek, Inc., a Johnson & Johnson
🏥 Medical Devices Class I - Dangerous
Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw
Proteus 235
Ion Beam Applications S.A.
🏥 Medical Devices Class I - Dangerous
It has been observed during testing that there could be clinically non-negligible amount of dark current (a well-known physics effect observed in cyclotron) in Pencil Beam Scanning (PBS) treatment mode when system is not irradiating between layers.
🏥 Medical Devices Class I - Dangerous
Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture catheters due to a potential problem. Venture RX (Model 5820), Venture OTW (Model 5821), and Venture CS (Model 5822) catheters. After an internal investigation, VSI determined that material used in catheter construction may detach from within the lumen of the distal tip during use.