State
72,907 recalls have nationwide distribution and so reach DC. 2,795 additional recalls listed District of Columbia specifically in their distribution scope.
Of the 2,795 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 946 (34%) are Severe.
Which agencies issued them
These figures cover only the 2,795 recalls whose distribution notice names District of Columbia specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.
Exacta Mix Vented Micro-Volume Inlet tubing sets are being recalled because affected lots may contain 0.8-micron filters in place of the validated 3-micron filters.
Albertsons store-made Cookies Cowboy 18 count is being recalled because the contains statement does not declare pecan. 982 units are affected.
The BD Pyxis Anesthesia Station 4000 is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
The BD Pyxis MedStation ES medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
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.
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 Shrimp 41-50 P&D with Cilantro Lime Marinade is being recalled because the contains statement does not declare shrimp and anchovy.
Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.
The Large Volume Pump of the Ivenix Infusion System is being recalled because of the potential for the Cassette Loading Lever to break. 18,444 installed bases are affected.
Albertsons store-made Cake Cakerie Strawberry Shortcake Triangle is being recalled because the contains statement does not declare hazelnut. 71 units are affected.
Philips Azurion 5M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable.
24/7 life by 7-Eleven 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 Ready Meals Meatloaf is being recalled because the contains statement does not declare anchovy. 353 units are affected.
The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Philips Azurion 3M12 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.
The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Haleon Tums Antacid Assorted Fruit Tablets, 750 mg, in 330-count bottles are being recalled because of the presence of small metallic particles in the chewable tablets.
Albertsons store-made Shrimp & Surimi Ceviche Fresh is being recalled because the contains statement does not declare sea bream. 315 units are affected.
Albertsons store-made Imitation Crab and Shrimp Salad Sriracha is being recalled because the contains statement does not declare pollock. 15 units are affected.
Philips Azurion 7B12/12 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 Platter Snack Chewie Susans Thumbprints is being recalled because the contains statement does not declare pecan. 158 units are affected.
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.
Albertsons store-made Banana Nut Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 434 units are affected.
Albertsons store-made Snacker Salad Tuna Pickle is being recalled because the contains statement does not declare tuna. Seven units are affected.