State

Maryland product recalls

72,971 recalls have nationwide distribution and so reach Maryland. 8,218 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total: 8,218
Critical: 996
Severe: 2,131
Most recent: 2026-09-09

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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7026–7050 of 81189

HighFDA (Devices)·Z-1791-2025·2025-05-28
SmartPath to Ingenia Elition X MRI Systems Alignment Error Recall
Philips is recalling SmartPath to Ingenia Elition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The alignment errors could affect image interpretation.
Product
Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1787-2025·2025-05-28
Check-Flo Performer Introducer Medical Device Recall Notice
Cook Incorporated is recalling Check-Flo Performer Introducer devices because some units from affected lots may contain an incorrectly sized introducer sheath.
Product
Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN) REF RCFW-14.0-0-38-30-RB, Order Number (GPN) REF G08957,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1785-2025·2025-05-28
True 3D Viewer Model EP-00003 Software Orientation Display Issue Recall
Echopixel's True 3D Viewer (Model EP-00003) with certain software versions can display ultrasound image orientation incorrectly, potentially leading to misdiagnosis or incorrect surgical planning.
Product
True 3D Viewer, Model: EP-00003
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1786-2025·2025-05-28
Check-Flo Performer Introducer medical device recall for incorrect sheath sizing
Cook Incorporated is recalling Check-Flo Performer Introducer devices (10.0Fr) because affected units may contain an incorrectly sized introducer sheath, which could compromise proper device function.
Product
Check=Flo Performer Introducer, 10.0Fr, Reference Part Number(RPN) REF RCFW-10.0-0-38-30-RB, Order Number (GPN) REF G08686,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0445-2025·2025-05-28
Indomethacin Extended-Release Capsules Recalled for cGMP Deviations
KVK Tech, Inc. is recalling Indomethacin Extended-Release Capsules USP, 75 mg (Lot #18400A) nationwide due to cGMP deviations. The recall affects approximately 9,107 bottles distributed nationwide.
Product
INDOMETHACIN — INDOMETHACIN (INDOMETHACIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0446-2025·2025-05-28
Phentermine Hydrochloride Capsules 30mg Recalled for cGMP Deviations
KVK Tech, Inc. is recalling 9,680 bottles of Phentermine Hydrochloride Capsules 30mg nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall is voluntary and firm-initiated.
Product
PHENTERMINE HYDROCHLORIDE — PHENTERMINE HYDROCHLORIDE (PHENTERMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1800-2025·2025-05-28
Ingenia 3.0T CX MRI System Alignment Error in Cross Reference Line
Philips is recalling the Ingenia 3.0T CX MRI system due to potential alignment errors in the cross reference line when using the MobiView application to review images. The alignment error could affect image accuracy during review.
Product
Product Name: Ingenia 3.0T CX; Model Number: 781271;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1799-2025·2025-05-28
Philips Ingenia 1.5T CX MRI System Alignment Error Potential
Philips is recalling Ingenia 1.5T CX MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application. This could affect image interpretation.
Product
Product Name: Ingenia 1.5T CX; Model Number: 781262;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0443-2025·2025-05-28
Esomeprazole Magnesium oral suspension recalled for failed impurity specifications
Zydus Pharmaceuticals is recalling Esomeprazole Magnesium delayed-release oral suspension, 20 mg, due to out-of-specification test results for unknown degradation products detected during long-term stability testing.
Product
ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1798-2025·2025-05-28
Ingenia Ambition S MRI devices recalled for alignment errors
Philips is recalling certain Ingenia Ambition S MRI devices due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1790-2025·2025-05-28
Philips SmartPath to dStream Medical Imaging Software Alignment Error
Philips is recalling SmartPath to dStream for XR and 3.0T medical imaging software due to potential alignment errors in cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1793-2025·2025-05-28
Evolution Upgrade 1.5T imaging system alignment error recall
Philips Evolution Upgrade 1.5T medical imaging systems may display alignment errors in cross-reference line functionality when reviewing images via MobiView application.
Product
Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1792-2025·2025-05-28
Philips Upgrade to MR 7700 Medical Device Alignment Error Recall
Philips is recalling the Upgrade to MR 7700 (Model 782130) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The misalignment could affect diagnostic accuracy.
Product
Product Name: Upgrade to MR 7700; Model Number: 782130;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1797-2025·2025-05-28
Ingenia 3.0T MRI Systems Recalled for Image Alignment Errors
Philips is recalling certain Ingenia 3.0T MRI systems worldwide due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1796-2025·2025-05-28
Philips Ingenia 1.5T S MRI System Alignment Error Recall
Philips is recalling the Ingenia 1.5T S magnetic resonance imaging (MRI) system due to potential alignment errors in cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia 1.5T S; Model Number: 781347;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1806-2025·2025-05-28
Smith & Nephew Lag/Compression Screw Kit Undersized Socket Defect
Smith & Nephew is recalling a Lag/Compression Screw Kit (REF: 71642690) because some compression screws have undersized hexagon sockets that render them non-functional and require replacement.
Product
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1802-2025·2025-05-28
Philips Ingenia Elition S MRI System Alignment Error Recall
Philips is recalling certain Ingenia Elition S MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1803-2025·2025-05-28
Philips Ingenia Elition X MRI System Alignment Error Recall
Philips has recalled specific Ingenia Elition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1804-2025·2025-05-28
MR 5300 Medical Device Recall for Cross Reference Line Alignment Error
Philips is recalling MR 5300 medical devices (Model Numbers 782110 and 782152) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1794-2025·2025-05-28
Philips Evolution Upgrade 3.0T MRI Cross Reference Line Alignment Error
Philips is recalling Evolution Upgrade 3.0T MRI systems (Models 782117 and 782143) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1788-2025·2025-05-28
Philips SmartPath to dStream 1.5T medical device alignment recall
Philips is recalling certain SmartPath to dStream 1.5T medical imaging devices due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1795-2025·2025-05-28
Ingenia 1.5T MRI Systems Recalled for Alignment Errors
Philips is recalling Ingenia 1.5T MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25T009000·2025-05-27
Sailun Recalls Transamerican Tires Due to Sidewall Puncture Risk
Sailun is recalling specific Transamerican tires because a sidewall puncture may cause air leaks, increasing the risk of a crash.
Product
TIRES:SIDEWALL recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V351000·2025-05-27
Kia K5 parking lights can flicker due to a software error
Kia is recalling certain 2025 K5 vehicles because a software error in the Power-net Domain Controller may cause the parking lights to flicker, failing FMVSS 108.
Product
KIA — KIA K5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E040000·2025-05-26
Micro DOT Recalls Blister and Twister Helmets for Penetration Protection Defect
Micro DOT Helmet Co. is recalling Blister and Twister helmets because they may lack proper penetration protection, increasing injury risk in crashes.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide