State

Maryland product recalls

72,982 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 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7101–7125 of 81200

HighFDA (Food)·F-0778-2025·2025-05-21
President Brand Kumquat Slices Recalled for Undeclared Sulfites
East CK Trading Inc. is recalling President Brand Kumquat Slices because they contain undeclared sulfites. Sulfites are a known allergen that can cause serious reactions in sensitive individuals.
Product
PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK TRADING INC.; INGREDIENTS: Kumquat slices; packaged in clear plastic jars with UPC 8 10077 20936 3
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1773-2025·2025-05-21
Philips Intera 1.0T MRI Quadrature Body Coil Seal Failure Recall
Philips is recalling Intera 1.0T Power/Pulsar MRI systems (Model 781103) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and injure patients during scanning.
Product
Intera 1.0T Power/Pulsar, Model Number: 781103;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1780-2025·2025-05-21
Philips Intera 3.0T Quasar Dual MRI Scanner Coil Seal Adhesive Failure
Philips is recalling the Intera 3.0T Quasar Dual MRI scanner (Model 781150) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 3.0T Quasar Dual, Model Number: 781150;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1779-2025·2025-05-21
Philips Intera 1.5T R11 MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.
Product
Intera 1.5T R11, Model Number: 781170;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Quadrature Body Coil Seal Failure
Philips is recalling the Intera 1.5T Omni/Stellar MRI scanner due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and cause patient injury. The loose seal during scanning could result in skin abrasions, bruises, lacerations, hair loss, or tissue damage.
Product
Intera 1.5T Omni/Stellar, Model Number: 781104;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1781-2025·2025-05-21
Philips Intera CV MRI Quadrature Body Coil Seal Adhesive Failure Recall
Philips is recalling Intera CV MRI units (Model 781107) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning, including skin abrasions, lacerations, or tissue damage.
Product
Intera CV, Model Number: 781107;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2025·2025-05-21
Philips Intera 1.0T MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.0T Omni/Stellar MRI systems (37 units: 3 in US, 34 internationally) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that can cause skin injuries during patient scanning.
Product
Intera 1.0T Omni/Stellar, Model Number: 781102;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2025·2025-05-21
Philips Intera 1.5T MRI Scanner QBC Seal Adhesive Failure Risk
Philips is recalling the Intera 1.5T Power/Pulsar MRI scanner because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 1.5T Power/Pulsar, Model Number: 781105;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1766-2025·2025-05-21
Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk
Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2025·2025-05-21
Philips Intera 0.5T Standard MRI System Quadrature Body Coil Seal
Philips is recalling the Intera 0.5T Standard MRI system (Model 781101) because the Quadrature Body Coil seal adhesive may fail and create sharp edges that could injure patients during scanning.
Product
Intera 0.5T Standard, Model Number: 781101;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0777-2025·2025-05-21
Kasundi Peeled Mango Pickle in Oil recalled for elevated lead levels
Advance Food International Inc. is recalling Kasundi Peeled Mango Pickle in Oil due to elevated lead levels detected in the product. The affected product was distributed in the Northeast.
Product
National brand Kasundi PEELED MANGO PICKLE IN OIL; Net Wt.: 1 Kg (35.27 oz)/ 2.20lb; Ingredients: Kasundi (Peeled Mango), Canola Oil, Cabbage, Salt, Mixed Spices, Vinegar, Sodium Benzoate as preservative; Product of Pakistan; packaged in a plastic jar with a red lid
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1752-2025·2025-05-21
Pruitt Irrigation Occlusion Catheter Recalled for Incomplete Sterile Seals
LeMaitre Vascular is recalling Pruitt Irrigation Occlusion Catheters (Catalog Numbers 2102-09, E2102-09) due to incomplete sterile barrier seals found during internal testing. The defect affects approximately 26,872 units distributed nationwide and internationally.
Product
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2025·2025-05-21
KliniTray surgical alignment system recalled for microbial contamination risk
Klinika Medical is recalling the KliniTray tissue resection margin examination board (Model 2001105-F) due to potential microbial contamination. The device was distributed nationwide in Massachusetts.
Product
KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and posi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1748-2025·2025-05-21
Abbott Alinity m Resp-4-Plex Amplification Kit Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex Amplification Kit due to reports of reactive negative controls and false positive results in respiratory virus testing.
Product
Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the qualitative detection and differentiation of RNA from influenza A virus (flu A), influenza B virus (fl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1743-2025·2025-05-21
Halyard RAPIDES E-PACK Cardiovascular Procedure Kit Surgical Needle Coating Issue
AVID Medical is recalling Halyard RAPIDES E-PACK Cardiovascular Procedure Convenience Kits due to a raw material defect in surgical needle coating that may cause diminished performance or coating removal during use.
Product
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V334000·2025-05-21
Volkswagen Atlas rearview camera image can become distorted in reverse
Volkswagen is recalling certain 2024-2025 Atlas and Atlas Cross Sport vehicles because a software error may distort the rearview camera image when the vehicle is in reverse.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V333000·2025-05-21
Mack Recalls 2026 MD Trucks Due to Incorrect Seat Belt Routing
Mack Trucks is recalling 2026 MD vehicles because the center bench seat belt assembly may be routed incorrectly, potentially failing to restrain occupants in a crash.
Product
MACK — MACK MD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V330000·2025-05-21
Ram ProMaster rearview camera image may not display in reverse
Chrysler is recalling certain 2022-2025 Ram ProMaster vehicles because a software error in the security gateway module may prevent the rearview camera image displaying, failing FMVSS 111.
Product
RAM — RAM, BRAUN PROMASTER, RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1761-2025·2025-05-21
Augmedics Perc Pin Adaptor component recalled due to design defect
Augmedics Ltd. is recalling the Perc Pin Adaptor, a component of the xvision Spine surgical navigation system, because the tightening knob is inconvenient to use and the tightening markings are improperly placed.
Product
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is designed to assist surgeons in placing pedicle screws accurately, during open or percutaneous computer-assisted spinal surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0419-2025·2025-05-21
La Roche-Posay Effaclar Duo Acne Treatment Recalled for Benzene
L'Oreal USA is voluntarily recalling all lots of La Roche-Posay Effaclar Duo Dual Action Acne Treatment due to detected trace levels of benzene in a specific lot.
Product
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40 mL (1.35 fl. oz.) Tube per Carton, La Roche-Posay LLC, 10 Hudson Yards, New Yor
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1747-2025·2025-05-21
FoundationOne Companion Diagnostic reports clinically relevant variants requiring amendment
Foundation Medicine is recalling four FoundationOne Companion Diagnostic (F1CDx) test reports sent to customers that contained clinically relevant variants requiring amendment, including one with an incorrect negative companion diagnostic claim.
Product
FoundationOne Companion Diagnostic (F1CDx)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0417-2025·2025-05-21
La Roche-Posay Effaclar Duo Acne Treatment Recalled for Benzene Contamination
La Roche-Posay Effaclar Duo acne treatment is being recalled due to detected trace levels of benzene. The recall affects 2,226,801 units distributed nationwide.
Product
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1765-2025·2025-05-21
Centurion Sterile Weitlaner Retractor recalled for packaging puncture risk
Medline Industries is recalling Centurion Sterile Weitlaner Retractors (2,100 units) due to potential puncture damage to sterile packaging. The defect could compromise the sterility of the surgical instrument.
Product
Centurion Sterile Weitlaner Retractor, Reorder: 67315
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1745-2025·2025-05-21
Contour Gold Eyelid Weight implants recalled for mislabeling
Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3012) due to mislabeling. Thirty-four weights distributed nationwide are affected.
Product
Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight, 1.2 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1741-2025·2025-05-21
Halyard CHRIST SUTURE KIT surgical needles coating defect recall
AVID Medical is recalling Halyard CHRIST SUTURE KIT units due to a raw material issue in the needle coating that may cause silicone to be removed during use, potentially affecting surgical performance.
Product
Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
Category
Medical Device
Distribution
Distributed nationwide