Jaime's Foods ATX Expands Jalapeno Ranch Recall to Additional Lot Codes
The FDA's enforcement report lists six identifying codes for the Austin firm's 16 oz. Jalapeno Ranch jars, recalled over an undeclared egg allergen.
Recalls & Safety Alerts in Texas
Every recalls & safety alerts report published for Texas, newest first.
Whole Foods Spicy Guacamole Dip Recall Expanded to Include Additional PLU Codes
The FDA has expanded its Class I recall of Whole Foods Spicy Guacamole Dip No Tomatoes over possible Salmonella contamination, adding new PLU codes to the list of affected products.
Whole Foods Spicy Guacamole Dip Recalled Over Possible Salmonella Contamination
FDA classifies recall as Class I, citing jalapenos that may be contaminated with Salmonella.
Dairyland Produce Recalls Jalapeño Peppers Over Possible Salmonella Contamination
The FDA has classified the recall as Class I, indicating a reasonable probability of serious health consequences.
FDA Reports Closure of Whole Foods Mild Guacamole Dip Recall Over Salmonella Risk
The FDA's August 26, 2026, enforcement report lists the Class I recall of Whole Foods Mild Guacamole Dip No Tomatoes as closed, following possible Salmonella contamination.
FDA Reports Class I Recall of Whole Foods Pomegranate Guacamole Dip Over Salmonella Risk
On August 26, 2026, the FDA reported a Class I recall of Whole Foods Pomegranate Guacamole Dip, initiated August 7, 2026, due to possible Salmonella contamination.
Whole Foods Medium Pico de Gallo Guacamole Dip Recalled Over Possible Salmonella
FDA classifies recall as Class I due to potential Salmonella contamination in jalapenos used in the product.
FDA Class II Recall Issued for Boston Scientific Transcarotid/Peripheral Access Kits
Galt Medical Corporation recalls 114,260 kits due to risk of black depth markings detaching from the sheath; no identifying codes provided in notice.
FDA Closes Class I Recall of Victory Medical Center Pharmacy Glutathione Vials
The agency considers the recall carried out; the product remains identified by lot numbers and use-by date.
FDA Reports Class II Recall of Argon Medical Devices Catheters
The FDA published an enforcement report for a recall of 20 catheters due to potential cracking and leaking at the hub.
FDA Closes Recall of Hondashi Seasoning Over Unlabeled Fish Allergen
The agency has closed its enforcement action for Pack'n Fresh LLC's Hondashi seasoning, considering the recall carried out.
Orthofix U.S. Recalls 48 Minirail External Fixation Devices Over Mislabeling
An FDA enforcement report dated July 22, 2026 records a Class II recall of the Orthofix MINIRAIL standard lengthener after devices were labeled with the wrong model numbers.
FDA Lists Class I Recall of Bulk Smoked Sausage Seasoning Over Undeclared Sesame
An enforcement report records an ongoing recall of 120 units of Adams Extract & Spice LLC seasoning distributed in Texas.
FDA Records Class I Recall of Adams Extract Hot Links Seasoning Over Undeclared Sesame
The agency's enforcement report lists 81 units of EC Hot Links Seasoning distributed in Texas, with the recall status ongoing.
FDA Records Ongoing Nationwide Class II Recall of 43 Million ChloraPrep Clear Applicators
An enforcement report cites a lack of assurance of sterility, saying affected applicator packaging may have an open or incomplete seal.
FDA Records Class II Recall of 167 Medtronic Neurosurgery Ventriculostomy Kits Over Endotoxin Levels
An FDA enforcement report lists an ongoing recall, initiated 17 June 2026, of a single lot of a sterile neurosurgical drainage kit distributed in 12 listed US states and Costa Rica.