State

Maryland product recalls

72,820 recalls have nationwide distribution and so reach Maryland. 8,217 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total: 8,217
Critical: 996
Severe: 2,130
Most recent: 2026-09-02

Of the 8,217 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 2,130 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,217 recalls whose distribution notice names Maryland specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

351–375 of 81037

SevereFDA (Food)·H-1205-2026·2026-08-12
Clover Hill Dairy Mild Cheese Varieties Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling various mild cheese varieties because they may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Mild Cheese Variety (Yummy Cheddar, White Cheddar, White Colby, Monterey Jack, Marble Jack). Sold in 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Food)·H-1216-2026·2026-08-12
Smoked Cheddar Cheese Varieties Recalled Due to Listeria Contamination
Clover Hill Dairy is recalling its smoked cheddar cheese varieties because they may be contaminated with Listeria monocytogenes. The products were sold in Maryland, Virginia, and New York.
Product
Clover Hill Dairy LLP, Smoked Cheddar Cheese Varieties (Cheddar, White Cheddar). Sold in 1/2-lb and 1-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2835-2026·2026-08-12
Therabody Theragun G4 PRO Charger Recalled for Fire Risk
Therabody is recalling Theragun G4 PRO chargers because they may overheat, presenting a risk of fire, smoke, or melting.
Product
Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO Black US - Refurb., SKU TG02428-01 G4 PRO NA, SKU G4-PRO-PKG-NA G4-PRO-PKG-US, SKU G4 PRO US G4 PRO Black US - Refurb V, SKU TG0002428
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0744-2026·2026-08-12
Cyclophosphamide Injection Recall: Stainless Steel Particulate Matter Found
Cyclophosphamide for Injection, USP, 2 gram/vial, is being recalled due to the presence of particulate matter identified as stainless steel. The recall affects 1,464 vials distributed nationwide.
Product
Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2850-2026·2026-08-12
Quantum Rehab Q6 Edge 4 Wheelchairs Recalled Due to Controller Software Issue
Pride Mobility Products Corp. is recalling Quantum Rehab Q6 Edge 4 powered wheelchairs because a software issue can cause unexpected braking and potential injury.
Product
Brand Name: Quantum Rehab Product Name: Q6 Edge 4 Model/Catalog Number: Q6 Edge 4 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2909-2026·2026-08-12
Blom-Singer Voice Prosthesis Boxes Mislabeled with Wrong Flange Type
Freudenberg Medical is recalling 12 Blom-Singer Classic Indwelling Voice Prosthesis devices because the boxes are mislabeled, swapping Large Esophageal Flange and Large Esophageal and Tracheal Flange contents.
Product
Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LEF
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1201-2026·2026-08-12
Soft Cuajada in Brine Recalled Due to Listeria monocytogenes Contamination
Clover Hill Dairy, LLC is recalling Soft Cuajada in Brine because it may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Soft Cuajada in Brine, sold in five (5) gallon and two (2) gallon buckets. Unknown information: labeling. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2897-2026·2026-08-12
United Orthopedic U2 Knee Implant Bushings Recalled Over Engraving Design Issue
United Orthopedic Corp. is recalling three Femoral offset bushing components of the U2 Total Knee System due to a design issue causing incorrect engraved numbering that could lead to incorrect implant orientation during surgery.
Product
Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1214-2026·2026-08-12
Clover Hill Dairy Pepper Jack Cheese Varieties Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling certain Pepper Jack Cheese Varieties because they may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (Snack Pack Assorted Pepperjack Stix (Jalapeno Cheddar, Pepper Jack)). Sold in approximate 0.40-lb (6.4oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereNHTSA·26V525000·2026-08-12
BMW Vehicles Recalled Due to Potential Loss of Power and Rollaway Risk
BMW is recalling certain 2021–2026 BMW models because the connection between the driveshaft and rear differential may become damaged, potentially causing a loss of power or vehicle rollaway.
Product
BMW — BMW 750E XDRIVE, 840I, 840I XDRIVE, 540I
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-1208-2026·2026-08-12
Fresh Cheddar Curd Cheese Recalled Due to Listeria Contamination
Clover Hill Dairy's Fresh Cheddar Curd cheese is recalled due to Listeria monocytogenes contamination. The product was distributed in Maryland, Virginia, and New York.
Product
Clover Hill Dairy LLP, mild cheese variety (Fresh Cheddar Curd). Sold in approximate 0.75-lb and 1.5-lb box units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2840-2026·2026-08-12
Radial Jaw 4 Jumbo Biopsy Forceps Packaging Sterile Barrier Recall
Boston Scientific is recalling Radial Jaw 4 Jumbo Biopsy Forceps due to potential breach in the sterile barrier of device packaging. The recall affects 5,020 units in the US and 20,770 units outside the US.
Product
Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240cm Box 5; Outer Box UPN: M00513363; Inner Box UPN: M00513360.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1215-2026·2026-08-12
Clover Hill Dairy Pepper Jack Cheese Varieties Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling Pepper Jack Cheese Varieties due to potential Listeria monocytogenes contamination.
Product
Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (3-in-a-Pack Assorted Jalapeno Cheddar, Pepper Jack, Sizzling Colby). Sold in approximate 0.20-lb (3.2oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2862-2026·2026-08-12
Stryker AHTO Tube Set Packaging Recalled for Handpiece Leaking
Stryker is recalling 46,212 units of its AHTO Tube Set Packaging (Catalog Number 0250070600) due to reported complaints of leaking from the handpiece during use. The recall affects products distributed worldwide, including US Nationwide and multiple countries.
Product
STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2843-2026·2026-08-12
Powered Wheelchair Controller Software Recall by Pride Mobility
Pride Mobility is recalling 1,102 Q6 Edge 3 Stretto powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.
Product
Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Stretto Model/Catalog Number: Q6 Edge 3 Stretto Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1210-2026·2026-08-12
Clover Hill Dairy Sharp Cheese Snack Pack Sharp Stix Recalled Due to Listeria
Clover Hill Dairy, LLC is recalling Sharp Cheese Snack Pack Sharp Stix (White or Yellow) because they may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Sharp Cheese Snack Pack Sharp Stix White or Yellow. Sold in approximate 0.40-lb (6.4oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2856-2026·2026-08-12
Powered Wheelchair Control Software Recall by munevo
Munevo is recalling 19 powered wheelchair hands-free control systems due to a software issue that may cause the driving mechanism to fall out of calibration, leading to unexpected steering drift or imprecise control.
Product
munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2876-2026·2026-08-12
GE Healthcare MAC VU360 Electrocardiograph Software Recall
GE Healthcare is recalling 163 MAC VU360 electrocardiograph units due to a software issue that may cause a previous patient's data to remain visible and be incorrectly associated with a subsequent patient.
Product
GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1200-2026·2026-08-12
Smoked Pepper Cheese Varieties Recalled Due to Listeria monocytogenes Contamination
Clover Hill Dairy, LLC is recalling Smoked Pepper Cheese Varieties (Jalapeno Cheddar) because they may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Smoked Pepper Cheese Varieties (Jalapeno Cheddar), sold in 1/2-lb and 1-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2891-2026·2026-08-12
Philips Allura X-Ray Systems Recalled Over Unauthorized Hard Disk Drives
Philips is recalling 5,012 Allura interventional fluoroscopic X-ray systems nationwide due to potential loss of imaging functionality, motorized movement, or data caused by unauthorized hard disk drives.
Product
Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model Numbers: 722003, 722010, 722026. 2. Allura Xper FD10 OR Table; Model Number: 722033. 3. Allura Xper FD10/10; Model Numbers: 722005, 722011, 722027. 4. Allura
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2889-2026·2026-08-12
Beckman Coulter MicroScan Panel Update DVD Kits Recalled
Beckman Coulter is recalling MicroScan LabPro V5.03 Panel Update 11 DVD Kits due to incorrect algorithms that may affect antimicrobial susceptibility test results, potentially leading to false susceptibility classifications.
Product
REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following instruments: - B1018-280 MicroScan autoSCAN-4 Instrument - B1018-283 MicroScan WalkAway-40 plus Instrument - B1018-284 MicroScan WalkAway-96 plus Instrument - B1018-440 DxM-1040 MicroScan Walk
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2857-2026·2026-08-12
OXOS Medical Recalls MC2 Portable X-Ray Systems Over Circuit Board Overheating
OXOS Medical Inc is recalling 77 units of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The recall affects devices distributed nationwide in FL, GA, IN, SC, TX, and VA.
Product
Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Description: The MC2 Portable X-Ray System ( MC2 System or MC2 ) is a portable and handheld x-ray system designed to aid clinicians with po
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2842-2026·2026-08-12
Quantum Outback Powered Wheelchair Controller Recalled Due to Unexpected Braking Risk
Pride Mobility Products Corp. is recalling Quantum Outback powered wheelchairs due to a software issue that may cause unexpected braking and potential injury.
Product
Brand Name: Quantum Rehab Product Name: Quantum Outback Model/Catalog Number: Quantum Outback Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2841-2026·2026-08-12
Powered wheelchair controller recalled for unexpected braking hazard
Pride Mobility Products Corp. is recalling 1,102 Quantum 4Front 2 wheelchair controllers because reminder pop-ups can trigger unexpected park brake stops while driving, causing falls or injuries.
Product
Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2883-2026·2026-08-12
Knee Prosthesis Trial Recall for Manufacturing Defect
United Orthopedic Corp. recalls U2 Total Knee System PSA Box Trial due to a manufacturing defect in a component screw that prevents proper assembly of the stem trial.
Product
Brand Name: U2 Total Knee System Product Name: PSA Box Trial, L, #1-6 and PSA Box Trial, R, #1-6 Model/Catalog Number: 9323-5511 thru 9323-5516 and 9323-5521 thru 9323-5526 Software Version: N/A Product Description: Knee femur prosthesis trial, reusable Component: No, N/A
Category
Medical Device
Distribution
Distributed nationwide