Product has the potential to be contaminated with Salmonella.
All Recalls
95,064 total recalls in our database
Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag is both lot number and a stamped expiration date. UPC 719283 357212; 12-9oz retail units per case.
Ferris Coffee and Nut Company
Undeclared allergens (wheat and soy).
Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.
Products contain undeclared soy, specifically soy lecithin.
Foreign object (stainless steel dust/flakes or shreds of plastic)
Swad Orange Flavored Masala Candy
Raja Foods and Vegetables
Contains undeclared FD&C Yellow 6
Undeclared allergen ingredient (fish)
Foreign object (stainless steel dust/flakes or shreds of plastic)
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
Crystallization; identified as Buprenorphine free base
Failed Dissolution Specifications
Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B
Medline Industries
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
GE Medical Systems
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
Stryker Sustainability Solutions
Incomplete seals on sterile product
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to increased vessel wall stress, neointimal hyperplasia, vessel injury/rupture; if undersized may lead to incomplete expansion/malposition, acute stent thrombosis, distal embolization, ischemic neurological events
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Stryker Sustainability Solutions
Incomplete seals on sterile product
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
Potential for mislabeled syringe produced by the i.v.STATION device.
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Stryker Sustainability Solutions
Incomplete seals on sterile product