The Recall Desk

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.

27276–27300 of 81821

  • HighFDA (Devices)·Z-1927-2021·2021-06-30

    Cardiac assessment system may display test reports in wrong patient records

    GE Healthcare's Case Cardiac Assessment System and CardioSoft diagnostic application may display one patient's cardiac test report in another patient's medical record under certain conditions. No patient injuries have been reported.

    Product
    Case Cardiac Assessment System for Exercise Testing and CardioSoft Diagnostic System Exercise Stress Testing ECG application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0686-2021·2021-06-30

    Clio Vanilla Greek Yogurt Mini Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla Greek Yogurt Mini Bars due to the possibility of metal fragments in the product. Consumers should not consume affected yogurt bars.

    Product
    Clio Vanilla Greek Yogurt Mini Bars wrapped in a Chocolate Coating 6.2oz pouch x 6 pouches per case, UPC: 854021008077
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1932-2021·2021-06-30

    AeroChamber PLS Spacer Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling AeroChamber PLS spacers exposed to freezing temperatures during shipping, which may cause inaccurate drug delivery results. Affected units shipped between February and March 2021 in Florida, Georgia, and South Carolina.

    Product
    AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0693-2021·2021-06-30

    Clio Peach Less Sugar Yogurt Bars recalled for possible metal fragments

    Clio LLC is recalling Clio Peach Less Sugar Yogurt Bars due to the possible presence of metal fragments in the product. The 10-pack boxes with best buy dates between 2/7/2021 and 6/20/2021 were distributed nationwide.

    Product
    Clio Peach Less Sugar Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 854021008213
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0690-2021·2021-06-30

    Clio Honey Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Honey Greek Yogurt Bars due to the possibility of metal fragments in the product. The recall affects 5,423 cases distributed nationwide with best-by dates between March 7, 2021 and July 11, 2021.

    Product
    Clio Honey Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 861703000168
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V492000·2021-06-30

    2021 Volkswagen Jetta Air Bag Control Module Welding Defect Recall

    Volkswagen is recalling 2020-2021 Jetta vehicles because the air bag control module was welded in an incorrect position. This can cause air bags to deploy improperly during a crash or deploy unexpectedly, increasing injury risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0697-2021·2021-06-30

    Clio Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla and Strawberry Club pack Greek Yogurt Bars nationwide due to the possibility of metal fragments in the product. Consumers should not eat the affected bars.

    Product
    Clio Vanilla / Strawberry Club pack Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 12 , 16pc tray, 24g x 24 (12pc tray), 55g x 16 (8pc tray). UPC codes: 854021008121, 854021008138, and 854021008022
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1906-2021·2021-06-30

    SARS-CoV-2 IgG II Calibrator Results Potentially Multiplied by 1000

    Beckman Coulter's Access SARS-CoV-2 IgG II Calibrator may return test results inflated by up to 1000-fold due to software errors, potentially misrepresenting patient immune status.

    Product
    Access SARS-CoV-2 lgG II Calibrator, REF C69058, IVD, CE UDI: (01)15099590742751
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Food)·F-0692-2021·2021-06-30

    Clio Mixed Berry Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Mixed Berry Less Sugar Yogurt Bars due to possible metal fragments in the product. Consumers should not eat the affected bars and should contact the company or return them to the retailer.

    Product
    Clio Mixed Berry Less Sugar Yogurt Bars wrapped in a Chocolate Coating 10 Clio Retail 10-pack, UPC code: 854021008190
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1937-2021·2021-06-30

    OneTouch Ultrasoft Lancets recalled due to temperature exposure during shipping

    Cardinal Health is recalling 531 boxes of OneTouch Ultrasoft Lancets shipped February-March 2021 due to temperature exposure during shipment that may cause inaccurate test results.

    Product
    ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21157·2021-06-30

    Children's Nightgowns Recalled for Flammability Standard Violation

    About 4,900 Booph children's nightgowns sold on Amazon from March through June 2021 are being recalled because they fail to meet federal flammability standards for sleepwear, posing a burn risk to children.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0638-2021·2021-06-30

    Mephyton Phytonadione 5 mg Tablets Recall for Failed Impurity Specifications

    Bausch Health Companies is recalling Mephyton (Phytonadione) 5 mg tablets nationwide because certain lots failed impurities and degradation specifications. Affected consumers should contact their healthcare provider.

    Product
    Mephyton (Phytonadione) 5 mg tablets, 100-count tablets, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ, 08807, USA, NDC 0187-1704-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0702-2021·2021-06-30

    Favorite Day Caramel Cashew Trail Mix Recalled for Plastic Contamination

    John B. Sanfilippo & Son Inc. is recalling Favorite Day Caramel Cashew Trail Mix nationwide because the product may contain stringy pieces of flexible plastic.

    Product
    favorite day caramel cashew Trail Mix, Product Number 04312. Milk Chocolate caramel balls, cashews, M&M'S milk chocolate candies and Peanuts. Net Wt 14 oz. (396g), UPC 85239-15671
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1945-2021·2021-06-30

    Medical Action Industries Hemostats Recalled for Flaking Metal Defects

    Medical Action Industries is recalling Mosquito Hemostats due to potential flaking metal and brown spots on the devices. The recall affects 23 boxes of surgical instruments distributed nationwide.

    Product
    Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1942-2021·2021-06-30

    Blood Glucose Test Strips Recalled for Temperature Exposure During Shipping

    Cardinal Health is recalling ACCU-CHEK SMARTVIEW 100 test strips distributed in Florida, Georgia, and South Carolina due to temperature excursions during shipping that may cause inaccurate glucose readings.

    Product
    ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0636-2021·2021-06-30

    Diflorasone Diacetate Ointment recalled for foreign particles

    Teligent Pharma is recalling Diflorasone Diacetate Ointment USP 0.05% due to the presence of foreign particles found during routine stability testing. The recall affects 6,240 tubes distributed nationwide.

    Product
    Diflorasone Diacetate Ointment USP, 0.05%, packaged in a)15 g (NDC 52565-063-15) and b) 30 g (NDC 52565-063-30) tubes, Rx only, Manufactured by: Teligent Pharma, Inc, Buena, NJ 08310.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0701-2021·2021-06-30

    Favorite Day Peanut Butter Chocolate Trail Mix Recalled for Plastic Pieces

    John B. Sanfilippo & Son Inc. is recalling Favorite Day Peanut Butter Chocolate Trail Mix because some packages may contain stringy pieces of flexible plastic.

    Product
    favorite day peanut butter chocolate Trail Mix, Product Number 04315. Peanut butter cups, Milk Chocolate-covered cereal squares, peanuts, chocolate chips and Peanut Butter Chips. Net Wt 8 oz. (226g), UPC 85239-15683
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1935-2021·2021-06-30

    Vicks vaporizers recalled for temperature exposure during shipping

    Cardinal Health is recalling Vicks 1.5-gallon vaporizers exposed to temperature excursions during shipping delays in February-March 2021, which may cause inaccurate results. Affected units were distributed in Florida, Georgia, and South Carolina.

    Product
    VAPORIZER VICKS 1.5GAL Item Number: 2354942
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1943-2021·2021-06-30

    LED therapy device pads recalled for improper cord assembly and power failure risk

    Inlightened Partners LLC is recalling 926 inLight Medical LED Pads due to improper assembly of cord connectors, which may cause power interruptions and controller shutdown.

    Product
    inLight Medical LED Pads used with Polychromatic light technology system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0639-2021·2021-06-30

    Phytonadione 5 mg Tablets Recalled for Failed Impurity Specifications

    Bausch Health Companies is recalling Phytonadione 5 mg tablets distributed nationwide because the affected lots failed to meet impurity and degradation specifications. Consumers should consult their healthcare provider before stopping this medication.

    Product
    Phytonadione Tablets, 5 mg, 30-count ablets, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA, NDC 68682-170-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V489000·2021-06-29

    East Manufacturing Recalls 2018-2021 MMX Trailers for Steering Defect

    East Manufacturing is recalling 2018-2021 MMX trailers because the steering arm may detach, potentially causing loss of steering control and increasing crash risk.

    Product
    EAST MANUFACTURING — EAST MANUFACTURING MMX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E060000·2021-06-29

    Cummins Recalls L9 Diesel Engines Due to Excessive Ammonia Exhaust

    Cummins is recalling specific L9 Diesel Engines because software calibration may allow excessive ammonia into the tailpipe, increasing injury risk.

    Product
    ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:MANIFOLD/HEADER/MUFFLER/TAIL PIPE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V490000·2021-06-29

    2021-2022 VanLeigh Beacon RV Egress Window May Not Fully Open

    VanLeigh is recalling 2021-2022 Beacon recreational vehicles because a rear ladder can interfere with the rear egress window, preventing it from fully opening in emergencies.

    Product
    VANLEIGH — VANLEIGH BEACON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E059000·2021-06-29

    Aftermarket LED Headlight Bulbs Recalled for Excessive Glare

    Shenzhenshi Axi Technology is recalling OXILAM LED headlight bulbs sold on Amazon because they create excessive glare, failing federal safety standards.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V486000·2021-06-29

    Porsche Recalls 2020-2021 Taycan Models for Powertrain Software Fault

    Porsche is recalling certain 2020-2021 Taycan models due to a software monitoring fault that can incorrectly shut down the powertrain, causing loss of motive power and increasing crash risk.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide