State
73,817 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,378 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,605 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Harvard Drug Group is voluntarily recalling Rugby Calcionate Syrup due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Zydus Pharmaceuticals is recalling 44,800 bottles of 30mg Paroxetine tablets because foreign Risperidone tablets were found in the packaging.
The Harvard Drug Group is voluntarily recalling Rugby Ferrous Sulfate Liquid due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Monster Energy Company is recalling Java Monster Loco Moca Coffee & Energy because the product was distributed without undergoing the required retort step.
Bella Pharmaceuticals is recalling 7 vials of Methylcobalamin 10mg due to a lack of assurance of sterility. The product was distributed nationwide in the United States.
Leader Liquid Vitamin D Supplement for Breastfed Infants is being voluntarily recalled due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Bella Pharmaceuticals is recalling Magnesium Chloride 200mg vials because the company cannot ensure the product is sterile.
Bella Pharmaceuticals is recalling specific lots of Calcium chloride 10% vials because the company cannot ensure the product is sterile.
The Harvard Drug Group is voluntarily recalling Rugby Cerovite Liquid due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby D 3 Vitamin Liquid due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.
Porsche is recalling specific 2003-2006 Cayenne models because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.
Bella Pharmaceuticals is recalling specific lots of L-Glutamine 100mg vials because the company cannot guarantee the product is sterile.
Double K is recalling 2016-2017 Hometown Trolley buses because the seat belt buckle may be stuck in the locked position, preventing the belt from latching.
DEMDACO is recalling about 1,500 infant bib and bootie sets because rattle attachments can detach, posing a choking hazard. No injuries have been reported.
Zimmer Biomet is recalling 64 ROSA surgical device foot switches that may freeze or shut down during use.
REV Recreation Group is recalling 2013-2016 Fleetwood Bounder and Southwind RVs because insufficient battery tray welds may cause the tray to separate, risking fire or injury.
John Deere is recalling D105 lawn tractors and service transmissions because the transmission can fail, posing a crash hazard. No injuries have been reported.
Baxter Healthcare is recalling 164,700 units of Amia Automated Peritoneal Dialysis Sets due to increased customer complaints regarding flow and drain alerts.
Fireworks Over America is recalling Serious Spinout fireworks because the device can tip over and fire shells at bystanders, posing burn, fire, and impact hazards.
Mako Surgical Corporation is recalling the Makoplasty Partial Knee Application software because it may fail to display all necessary constants when the screen is full.
Toshiba American Medical Systems is recalling 140 Radrex-i digital radiography systems because a software error causes image loss and requires a system reboot.
Leica Biosystems Richmond Inc. is recalling four units of Podoplanin (D2-40 Mab) antibody because a delay in transit may have caused the product to be stored outside of required temperature limits.
Leica Biosystems Richmond Inc. is recalling three units of Glypican-3 (1G12 Mab) antibody because a delay in transit may have caused the product to be stored outside of defined temperature requirements.
Implant Direct Sybron is recalling 84 Guided Surgery Handle Kits because the 2.3mm drill guide inserts have a smaller inside diameter than specifications require.
Beckman Coulter is recalling 320 units of Sekisui Acetaminophen reagent because carryover from ACTH reagent may cause falsely elevated Lipase results on the AU 680 analyzer.