State
72,907 recalls have nationwide distribution and so reach Maryland. 8,218 additional recalls listed Maryland specifically in their distribution scope.
Of the 8,218 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,131 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,218 recalls whose distribution notice names Maryland specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline Pelvic Lap Packs are being recalled because representative samples did not meet applicable catheter performance specifications. 20 units are affected.
Medline Nursing Kits, SKU EDUC1044, are being recalled because representative samples did not meet applicable catheter performance specifications. 730 units are affected.
Medline CRANI procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 3,521 units are affected.
HeartMate 3 System Controllers, model 106531US, are being recalled due to 11 volt backup battery failures. 694 units are affected.
Lucky Super Soft Antifungal Athlete's Foot Cream, clotrimazole 1%, is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 1,102 tubes affected.
Medline EBSI central line, CVC/PICC/midline and dialysis dressing change kits are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Medline convenience kits for ACD, ACDF, ACL and ALIF procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
The Medline Labor & Delivery C-Section convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Chlorthalidone Tablets, USP, 25 mg, are being recalled because they failed dissolution specifications. 11,460 bottles are affected.
Medline da Vinci, general robotics and gynaecology laparoscopy convenience kits are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
HarmonyAIR A-Series Surgical Lighting Systems are being recalled because of the potential for paint delamination, meaning chipping or peeling, on the light heads. 4,138 units affected.
The Medline Hernia Repair Tote convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Medline convenience kits for ACL, arthroscopy, back and paediatric procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
The Medline Breast-Hernia-Port CDS-LF kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Medline central line dressing kits, PICC/CVC/midline CHG dressing kits, port-a-cath kits and vein ablation packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.
VistaPharm Kerr Insta-Char in an aqueous base, 25 grams activated charcoal, is being recalled because the product did not meet Over-the-Counter Monograph M023.
Medline C-section kits, packs and recovery kits are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Medline convenience kits including AV fistula, endovascular, EP device and aneurysm packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Medline convenience kits including basic packs, general laparoscopy, CVC insertion bundles and da Vinci packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.
directCHECK ACT-LR whole blood quality control, level 2, is being recalled because the assayed control carries labeling with an incorrect performance range. 6,060 units affected.
Lucky Super Soft First Aid Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 2,503 tubes are affected.
The Medline WT LAVH Pack is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Med Pride Hydrocortisone Cream 1%, 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,944 tubes are affected.
The Medline Femoral Block Tray is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Medline C-Section Kits and Packs are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.