State
72,919 recalls have nationwide distribution and so reach New York. 12,902 additional recalls listed New York specifically in their distribution scope.
Of the 12,902 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,133 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,902 recalls whose distribution notice names New York specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.
Kirkland Signature Ultra Strength Antacid, calcium carbonate 1000 mg, made by Guardian Drug Company for Costco, is being recalled over small metallic particles in the tablets.
Albertsons store-made Pistachio Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 354 units are affected.
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Market Basket Antacid, calcium carbonate 1000 mg ultra strength, is being recalled because of the presence of small metallic particles in the chewable tablets.
Philips Azurion 5M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Albertsons store-made Tray Charcuterie Elegant is being recalled because the contains statement does not declare pistachio. Eight units are affected.
Lannett Niacin Extended-release Tablets, 1,000 mg, are being recalled after a stability test returned an out-of-specification low result for Stage 3 dissolution at 24 hours.
Equaline Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.
Albertsons store-made Platter Brownies Assorted Seasonal is being recalled because the contains statement does not declare walnut. 15 units are affected.
TopCare Health Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Albertsons store-made Kitchen Salad Turkey Poppyseed is being recalled because the contains statement does not declare almond.
H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.
The Da Vinci 5 system tower is being corrected because the near infrared handheld camera can be unintentionally activated when a user tries to turn off illumination.
Wilco Peanut Co is recalling raw shelled peanuts (Runner Type) because they may contain undeclared tree nuts, posing an allergen risk to consumers with nut allergies.
Philips Azurion 7M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Casey's Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles in the tablets.
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles.
Discount Drug Mart Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
GE MAC 5 A4 and A5 Resting ECG Analysis Systems are being recalled because a development software version was released that can associate clinical information with the wrong patient.
Philips Azurion 7M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Albertsons store-made Shrimp & Surimi Ceviche Fresh is being recalled because the contains statement does not declare sea bream. 315 units are affected.