State

Maryland product recalls

73,596 recalls have nationwide distribution and so reach Maryland. 8,225 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total: 8,225
Critical: 994
Severe: 2,518
Most recent: 2026-10-21

Of the 8,225 recalls naming Maryland we have scored against our rubric, 994 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,518 (31%) are Severe.

Which agencies issued them

These figures cover only the 8,225 recalls whose distribution notice names Maryland specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27401–27425 of 81821

SevereFDA (Food)·F-0747-2021·2021-06-16
365 Everyday Value Whey Protein Powder Mislabeled with Soy Protein
365 Everyday Value Whey Protein Powder was mistakenly packaged with Soy Protein Powder. The affected canisters were distributed nationwide and may pose a risk to consumers with soy allergies.
Product
365 Everyday Value Whey Protein Powder Natural Vanilla Flavor, Net Wt. 13.9 oz. canisters, UPC 9948228764, Whole Foods Market 550 Bowie Street Austin, TX 78703. Store in a cool, dry place.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1798-2021·2021-06-16
Jelco Insulin Syringe Graduation Markings Recalled for Skew Defect
Smiths Medical recalls 1,432,200 Jelco insulin syringes with skewed graduation markings that could lead to incorrect dosing. Specific lot numbers are affected.
Product
JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G X 1/2" (0.33mm x 13mm), REF 4428-1 b) 1.0mL 29G X 1/2" (0.33mm x 13mm), REF 4429-1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1538-2021·2021-06-16
INNOVA SARS-CoV-2 Antigen Rapid Tests Recalled for Unauthorized Non-Clinical Distribution
INNOVA Medical Group is recalling SARS-CoV-2 antigen rapid test kits distributed to customers not enrolled in an authorized clinical investigation.
Product
For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Antigen *** SARS-CoV-2 Antigen Rapid Qualitative Test *** REF BT1309
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1833-2021·2021-06-16
DeRoyal Heart Cath Procedure Packs Recalled for Anesthetic Mislabeling
DeRoyal Industries is recalling 66 heart catheterization procedure packs due to mislabeling of anesthetic contents. The packs contain 0.5% Bupivacaine but are labeled as containing 1% Lidocaine, creating a medication error risk during surgery.
Product
DeRoyal Heart Cath Procedure Pack, REF 89-6556.08
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0674-2021·2021-06-16
BC Foods Celery Stalk and Leaf Dice Recalled for Salmonella
BC Foods is recalling Celery Stalk and Leaf Dice due to an ingredient testing positive for Salmonella. The product was distributed to food manufacturers and distributors across eight states.
Product
BC Foods Celery Stalk and Leaf Dice 3/8, AD Sulfites, 11 lb. Poly lined bulk fiber carton. Item code: VCE1-D38-AXG-AB-AR
Category
Food
Distribution
8 states
SevereFDA (Devices)·Z-1785-2021·2021-06-16
Avid Medical Fistula On-Off Kit Recalled for Potential Fungal Contamination
Avid Medical is recalling 720 Fistula On-Off Kits due to potential fungal contamination that may compromise package integrity. The BD ChloraPrep applicator component may develop Aspergillus penicillioides, which could contaminate other kit components.
Product
FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1787-2021·2021-06-16
Dialysis access kits recalled for potential fungal contamination risk
Avid Medical is recalling medical dialysis access kits due to potential fungal growth in an applicator component that may compromise the package seal and contaminate other components. Approximately 560 kits distributed nationwide are affected.
Product
DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1539-2021·2021-06-16
COVID-19 Self-Test Kit Distributed Without Clinical Investigation Authorization
Innova Medical Group recalled COVID-19 self-test kits distributed to customers outside of clinical investigation requirements. About 1,206 tests in 402 boxes were distributed across the U.S., Canada, India, and the United Kingdom.
Product
COVID-19 Self-Test Kit *** INNOVA *** 3T
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1832-2021·2021-06-16
DeRoyal Pacemaker Tray Mislabeled With Wrong Anesthetic Concentration
DeRoyal is recalling surgical procedure packs due to mislabeling. The product contains 0.5% Bupivacaine but is labeled as 1% Lidocaine, creating a medication identification error.
Product
DeRoyal Pacemaker Tray Pgybk, REF 89-6360.06
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1537-2021·2021-06-16
FDA Recalls Innova COVID-19 Self-Test Kits Due to Unauthorized Distribution
Innova Medical Group is recalling COVID-19 self-test kits distributed to customers outside an authorized clinical investigation. The recall affects 370 boxes of tests distributed nationwide and internationally.
Product
COVID-19 Self-Test Kit *** INNOVA *** 7T
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0748-2021·2021-06-16
Enoki Mushroom Recalled for Listeria monocytogenes Contamination
Rainfield Marketing Group is recalling 150g packages of Enoki Mushroom (UPC 085412004020) because samples tested positive for Listeria monocytogenes. The product was distributed to California, Texas, and Maryland.
Product
Enoki Mushroom, 150g clear plastic bag with orange bottom; UPC 085412004020 Product of Korea Do no consume Raw Distributed by Rainfield Marketing Group
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-1784-2021·2021-06-16
Adult Chest Tube Tray Recalled Due to Package Integrity Risk
Avid Medical is recalling 130 Adult Chest Tube Trays due to potential contamination from mold growth in a component. The BD ChloraPrep applicator may grow Aspergillus penicillioides, which could breach package integrity and contaminate other kit components.
Product
ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1805-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate Screw Mechanism Failure Recall
Alphatec Spine is recalling the Insignia Anterior Cervical Plate System because the screw blocking mechanism may disassociate during surgery or unlock afterward. Eight units were distributed across 15 states.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0122, Insignia, ACP, 1-Level, 22 mm, Rx Only, Non-Sterile, UDI: (01)00190376268484
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1831-2021·2021-06-16
Laboratory Software Device May Produce Erroneous Results from Inadequate Instructions
Normand Remisol Advance Data Manager versions 1.5–1.9 have insufficient instructions for proper rule programming and testing. User-written rules may not be properly validated, potentially leading to erroneous laboratory results.
Product
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS) and laboratory instruments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1802-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate Screw Blocking Mechanism Disassociation Recall
Alphatec Spine is recalling the Insignia Anterior Cervical Plate System due to a potential failure in the screw blocking mechanism that may disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0119, Insignia, ACP, 1-Level, 19 mm, Rx Only, Non-Sterile, UDI: (01)00190376268453
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1847-2021·2021-06-16
CooperSurgical Wallach Loop Electrode recalled for incorrect packaging
CooperSurgical has recalled its Wallach Loop Electrodes (Lot 274420) due to incorrect packaging. Packages labeled as Square Electrodes contained Round Electrodes instead, creating a risk of improper device use in surgical procedures.
Product
CooperSurgical Wallach Loop Electrode 10mm x 10mm Square P/N: 909131. Disposable Universal Electrodes, LOOP electrodes, used for electro-excisional procedures, and for electro-fulguration procedures of the lower genital tract
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-1812-2021·2021-06-16
Anterior Cervical Plate System Screw Mechanism May Fail Intraoperatively
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism that could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0242 Insignia, ACP, 2-Level, 42 mm, Rx Only, Non-Sterile, UDI: (01)00190376268415
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1844-2021·2021-06-16
Quanta System Sterile Optical Laser Fiber Recall for Potential Sterility Compromise
Quanta System is recalling 307 reusable sterile optical laser fibers nationwide due to potential sterility compromise. The affected devices were distributed through six U.S. distributors.
Product
Quanta System Sterile Optical Laser Fiber, reusable
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21151·2021-06-16
Cove Appliance 24-inch Built-in Dishwashers Recalled for Fire Hazard
Cove Appliance is recalling about 42,000 built-in dishwashers because the heating element can fail to shut off and overheat, creating a fire hazard. The company has received five reports of burning smells, flames, and smoking inside the dishwashers, though no injuries have been reported.
Product
Cove Appliance 24-inch built-in dishwashers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1804-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Recall: Potential Screw Mechanism Failure
Alphatec Spine is recalling 7 units of the Atec Insignia Anterior Cervical Plate System because the screw blocking mechanism could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0121, Insignia, ACP, 1-Level, 21 mm, Rx Only, Non-Sterile, UDI: (01)00190376268477
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1813-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System recall due to potential screw mechanism failure
Alphatec Spine is recalling Atec Insignia Anterior Cervical Plate System units due to a potential defect where the screw blocking mechanism may disassociate or unlock during or after surgery. No adverse events have been reported.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0244 Insignia, ACP, 2-Level, 44 mm, Rx Only, Non-Sterile, UDI: (01)00190376268507
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1838-2021·2021-06-16
Medical Device Software Defects in RayStation Treatment Planning System
RayStation radiation therapy treatment planning software versions 6 through 10A contain defects that may cause misleading dose evaluations and contouring errors. Healthcare facilities should verify treatment plans and contact the manufacturer for guidance.
Product
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.6 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 , 10.0.0.1154 , 10.0.1.52 or 10.1.0.613 .
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1820-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Screw Mechanism Recall
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to potential disassociation or postoperative unlock of the screw blocking mechanism during or after cervical spine surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0358 Insignia, ACP, 3-Level, 58 mm, Rx Only, Non-Sterile, UDI: (01)00190376268606
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2021·2021-06-16
Anterior cervical plate system screw mechanism may disassociate during or after surgery
Alphatec Spine's Atec Insignia Anterior Cervical Plate System has a potential defect where the screw blocking mechanism may disassociate during or after surgery, which could compromise spinal stabilization.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0118, Insignia, ACP, 1-Level, 18 mm, Rx Only, Non-Sterile, UDI: (01)00190376268446
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1803-2021·2021-06-16
Cervical Spine Plate System Screw Mechanism May Disassociate or Unlock
Alphatec Spine recalls its Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism, which may disassociate or unlock during or after spinal surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0120, Insignia, ACP, 1-Level, 20 mm, Rx Only, Non-Sterile, UDI: (01)00190376268460
Category
Medical Device
Distribution
Distributed nationwide