State
72,936 recalls have nationwide distribution and so reach New Mexico. 3,625 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,625 recalls naming New Mexico we have scored against our rubric, 747 (21%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 647 (18%) are Severe.
Which agencies issued them
These figures cover only the 3,625 recalls whose distribution notice names New Mexico specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Albertsons store-made Cake Yellow Fudge Pecan half 8-inch is being recalled because the contains statement does not declare pecan.
B. Braun SESK UPMC Double Catheter Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.
Albertsons store-made Cajun Salmon & Spanish Rice meal is being recalled because the contains statement does not declare salmon. 86 units are affected.
B. Braun BlockJocks Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable. 210 units are affected.
Covidien Mon-a-Therm Esophageal Stethoscopes with Temperature Sensor 400TM, REF 90042, are being recalled because the devices lack FDA clearance. 23,000 units are affected.
Albertsons store-made Ready Meals Tuna Salad & Pepper Jack Cheese Snacker is being recalled because the contains statement does not declare tuna. 293 units are affected.
B. Braun CESK Harris Methodist kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.
DeRoyal Industries Inc. is recalling Covaderm Plus Vascular Access Dressings because they lack sterility assurance.
Albertsons store-made Tortilla Crusted Tilapia is being recalled because the contains statement does not declare tilapia. 208 units are affected.
Covidien Shiley Tracheostomy Tubes with inner cannula, REF 6FEN, are being recalled following a customer complaint about incorrect display box labeling. 1,002 units are affected.
Albertsons store-made Shrimp P&D Cajun Seasoned is being recalled because the contains statement does not declare shrimp. 18 units are affected.
Albertsons store-made Salmon Atlantic Portion Piri Piri Marinade is being recalled because the contains statement does not declare salmon. 108 units are affected.
Albertsons store-made Shrimp Kabob 16-20 count with Kung Pao Marinade is being recalled because the contains statement does not declare shrimp.
Albertsons store-made Salmon Pesto with Asparagus is being recalled because the contains statement does not declare salmon. 149 units are affected.
B. Braun CESK Shands Jacksonville kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.
Albertsons store-made Shrimp 41-50 P&D with Jamaican Jerk Marinade is being recalled because the contains statement does not declare shrimp. Two units are affected.
Albertsons store-made Meal Salmon Cajun is being recalled because the contains statement does not declare salmon. 40 units are affected.
Albertsons store-made Shrimp Medium with Sweet Chili Marinade is being recalled because the contains statement does not declare shrimp. Four units are affected.
Albertsons store-made Gourmet Walnut Sticky Buns, 4 count, are being recalled because the contains statement does not declare walnut. 73 units are affected.
Albertsons store-made Cake Boston Almond is being recalled because the contains statement does not declare almond. Nine units are affected.
Albertsons store-made Shrimp P&D Old Bay Seasoned is being recalled because the contains statement does not declare shrimp. Five units are affected.
Albertsons store-made Salmon Kabob with Citrus Lemon Marinade is being recalled because the contains statement does not declare salmon.
Albertsons store-made Salmon Pot Rosettes & Rosemary is being recalled because the contains statement does not declare salmon. 95 units are affected.
HiRes Ultra 3D CI HiFocus Mid Scala cochlear implants are being recalled due to an incorrect shelf-life expiration date. 36 units are affected.
Eugia Lidocaine HCl Injection, USP 2% single-dose vials are being recalled because the label wrap covers the barcode, making it hard to scan. 168,300 vials are affected.