Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
All Recalls
95,018 total recalls in our database
Marketside Chopped Salad Kit Bacon Crunch UPC 681131305440
Dole Fresh Vegetables
Product has the potential to be contaminated with Listeria monocytogenes.
Signature Select, Athens, and Cal Pia brand Bread Butter White Bread 22 oz. loaf
Albertsons Companies
Foreign object; metal and plastic shavings.
Dole Premium Kit Endless Summer UPC 71430010730
Dole Fresh Vegetables
Product has the potential to be contaminated with Listeria monocytogenes.
Dole Cajun Ranch Chopped Kit UPC 71430002063
Dole Fresh Vegetables
Product has the potential to be contaminated with Listeria monocytogenes.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.
Super Chill Products
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Cross Contamination with Other Products:(mycophenolate mofetil).
Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01
Hikma Pharmaceuticals USA
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
Mckesson Medical-Surgical Inc. Corporate Office
Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.
TENSIVE Conductive Adhesive Gel, REF 016-401600
Natus Neurology
Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall related to their Tensive Conductive Adhesive Gel, Ref. 22-60 Lot Number A0623009. They have received five complaints. These customers reported that the gel is too thick, is discolored (darker than usual), and in one instance, patients reported irritation after procedures using the gel.
Observed outflow graft deformation known as Extrinsic Outflow Graft Obstruction (EOGO) associated with Left Ventricular Assist System.
smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS
Smiths Medical ASD
When a paraPAC plus ventilator is switched to the operating mode of VENTILATE, the ventilator may intermittently provide continuous positive gas flow instead of the intended cycling like a human breath. This non-cycling and continuous positive gas flow when in the cycling mode, is a malfunction, not allowing the ventilator to properly function as designed.
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case