State
73,100 recalls have nationwide distribution and so reach Maryland. 8,223 additional recalls listed Maryland specifically in their distribution scope.
Of the 8,223 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 8,223 recalls whose distribution notice names Maryland specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Yummy Swirly Ices Berry Blast popsicles are recalled due to undeclared milk allergen. Recall affects 262 boxes distributed across nine states.
Yummy brand Swirly Ices Fruity Melon popsicles are being recalled because they contain undeclared milk, a common allergen. The recall affects 268 boxes distributed to retail supermarkets in nine states.
Yummy brand Swirly Ices Tropical Tornado popsicles are recalled due to undeclared milk. The recall affects 275 boxes distributed to retail supermarkets in nine states.
Felling Trailers is recalling 2011-2022 Avtron D40548 trailers because the axle bracket may crack and break, allowing the axle to detach.
Yummy brand Swirly Ices popsicles are recalled due to undeclared milk allergen. The recall affects 282 boxes distributed across nine states.
Prime Food brand steam buns may contain undeclared sesame, an allergen not listed on the product label. The FDA classified this as a Class I recall affecting 477 cases across multiple U.S. states and international locations.
Prime Food Processing Corp. is recalling Prime Food brand Steam Buns because they may contain undeclared sesame, an allergen. Consumers with sesame allergies should not consume the product.
Agfa is recalling 141 DR 800 Digital Radiography X-ray systems for potential failure of the table's front lever chain.
Beaver Visitec International voluntarily recalled BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The recall affects 69 units distributed nationwide.
A software issue in DxI 9000 Access analyzers connected to laboratory automation systems may prevent processing of all samples, flagging tests as timed out and potentially delaying patient results.
Beaver Visitec International voluntarily recalls BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The recall affects 351 units distributed nationwide.
Intuitive Surgical is recalling the Ion Endoluminal System due to potential screw failure in the instrument cart arm, which could cause uncontrolled catheter motion in patient airways.
Dr. Reddy's Laboratories is recalling 31,802 bottles of IBU Ibuprofen 600mg tablets due to failed impurity specifications. The product was distributed nationwide and in Puerto Rico.
Stryker Corporation is recalling the iBur 3.0mm Precision Match Head surgical burr because it may generate higher-than-specified temperatures during use, potentially causing thermal injury that may require medical intervention.
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The recall affects 123 units distributed nationwide.
Volkswagen is recalling 2021-2024 ID.4 vehicles because door handles may allow water to enter the circuit board, causing doors to open unexpectedly while driving. Owners should contact Volkswagen dealers for free inspection and repair.
Beaver Visitec International recalls BVI CustomEyes Procedure Packs containing defective Sol-M syringes. About 1,756 units were distributed nationwide due to manufacturing defects.
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs because they contain Sol-Millennium Medical syringes that are subject to a manufacturer recall. A total of 103 units were distributed nationwide.
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M syringes distributed nationwide. The recall affects 35 units with Part Number 584770 and is classified as FDA Class II.
OrthoPediatrics Canada is recalling FRT250 cartridges used in the Fassier-Duval Telescopic IM System because an incorrect component was substituted during assembly.
Stryker recalls iBur 3.0mm Precision Round surgical burs due to potential for excessive temperatures where the bur shank meets the bushing. Thermal injury risk may require medical intervention.
Stryker iBur 4.0mm Diamond Round surgical burs may reach temperatures higher than specified, potentially causing thermal injury or tissue damage during bone-cutting procedures. Approximately 1,706 affected units have been distributed worldwide.
Beaver Visitec International is recalling 227 units of BVI CustomEyes Procedure Packs containing syringes from Sol-Millennium Medical due to a quality concern affecting those syringes.
Stryker iBur 4.0mm precision surgical burs may overheat where the shank meets the distal bushing. Excessive heat could cause minor tissue damage or thermal injury requiring medical intervention.
Beaver Visitec International, Inc. is recalling BVI CustomEyes Procedure Packs containing Sol-M manufactured syringes. The voluntary recall affects approximately 1,629 units distributed nationwide.