State
73,190 recalls have nationwide distribution and so reach Maryland. 8,224 additional recalls listed Maryland specifically in their distribution scope.
Of the 8,224 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 2,134 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,224 recalls whose distribution notice names Maryland specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wegmans Harissa Hummus (10.5 oz) is recalled because it contains undeclared sesame, an allergen. Consumers with sesame allergies who have purchased affected lots should not consume the product.
LQNN Inc. is recalling 222,320 bags of Vegetarian Pia Cake Mung Bean Pumpkin because the product contains undeclared egg allergen. Consumers with egg allergies should not eat this product.
Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits because they contain a sterile pre-filled syringe that was subsequently recalled by Nurse Assist. Approximately 10,808 units have been distributed worldwide.
LQNN Inc. is recalling BANH PIA Hopia Cake due to undeclared egg allergen. Approximately 222,320 bags were distributed to 31 U.S. states and Canada.
Taylor Fresh Foods recalls COLD CASE roasted street corn salad due to potential Listeria monocytogenes contamination. Affected: 60 cases across 28 states.
LQNN Inc. is recalling approximately 222,320 bags of Vegetarian Pia Cake Black Sesame Durian due to undeclared egg. Consumers with egg allergies should not consume this product.
Textron is recalling 2024 Cushman Hauler Pro LSV vehicles because a dump bed latch may crack or puncture the battery case, increasing the risk of a fire.
LQNN Inc. is recalling BANH PIA Hopia Cake Mungbean Durian due to undeclared egg allergen. The product was distributed to customers in 31 U.S. states and Canada.
LQNN Inc. is recalling 222,320 bags of Vegetarian Pia Cake Pandan Durian due to undeclared egg allergen. Consumers with egg allergies should not consume this product.
BANH PIA Liu Sha Pumpkin Pia Cake is recalled because it contains egg that is not declared on the label. The recall affects 222,320 bags distributed across 31 US states and Canada. Consumers with egg allergies should not consume this product.
Taylor Fresh Foods is recalling Marketside Bacon Ranch Crunch Chopped Salad Kits due to potential Listeria monocytogenes contamination. Affected products with best-by dates on or before Feb 21, 2024 were distributed to 28 states.
T Marzetti Co is recalling Chick-fil-A Polynesian Sauce Cups (28g single serve) due to undeclared wheat and soy allergens. The product was distributed across 11 U.S. states.
LQNN Inc. is recalling Banh Pia Classic Hopia because it contains undeclared egg allergen, which can cause serious allergic reactions. About 222,320 bags were distributed across 31 U.S. states and Canada.
LQNN Inc. is recalling Vegetarian Pia Cake Red Bean Durian products due to undeclared egg allergen. The recall affects 222,320 bags distributed across 31 U.S. states and Canada.
Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits containing a sterile pre-filled syringe that was recalled by Nurse Assist. Approximately 53,126 units were distributed worldwide.
Ortho-Clinical Diagnostics is recalling VITROS immunodiagnostic analyzer systems that may aspirate unintended sample containers during processing, potentially causing erroneous test results.
Howmedica Osteonics Corp. is recalling the NO 3 Triathlon TS Plus Tibial Insert due to potential breaches in the sterile packaging. The breaches could compromise product sterility and safety.
A software defect in VITROS 4600 Chemistry Systems causes quality control baselines to not update when users change them, potentially causing erroneous patient results.
A software defect in VITROS XT 3400 Chemistry Systems prevents quality control rules from properly reporting failures in test controls. This may result in erroneous patient test results being reported.
A software defect in VITROS 4600 Chemistry Systems running software versions 3.8.0 or 3.8.1 prevents quality control rules from being flagged or reported correctly, potentially allowing erroneous patient results to be released.
Synthes recalls 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails (5 units) due to failed sterilization. These surgical implants were distributed worldwide and pose infection risk if implanted.
FUJIFILM is recalling Synapse PACS Version 7.2.100 because the medical imaging software produces incorrect measurements when analyzing certain breast images. Affected healthcare facilities using this software version should verify measurement accuracy in their systems.
Synthes is recalling 11 TFNA Femoral Nails due to sterility failures. The affected units worldwide cannot be confirmed as sterilized and pose infection risks to patients.
Ortho-Clinical Diagnostics is recalling the VITROS XT7600 Integrated System due to potential aspiration from unintended sample containers during processing, which may result in erroneous test results. The recall affects 1,720 units distributed worldwide.
Synthes is recalling 47 VA-LCP Clavicle Plate 2.7 bone fixation implants (Lot 1201P12) distributed worldwide because sterility cannot be confirmed. Non-sterile surgical implants pose risk of infection.