State

Maryland product recalls

20,364 recalls have nationwide distribution and so reach Maryland. 0 additional recalls listed Maryland specifically in their distribution scope.

About recalls in Maryland

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Maryland consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

13551–13575 of 20364

SevereFDA (Devices)·Z-1357-2023·2023-04-26
Shiley Adult Flexible Tracheostomy Tubes Recalled Due to Undersized Connectors
Covidien is recalling Shiley Adult Flexible Tracheostomy Tubes due to undersized connectors that create loose connections with 15mm respiratory circuit components. Unsecure connections could cause respiratory failure, difficulty breathing, treatment delays, or serious injury.
Product
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner Cannula (REF, Product Description): 10CN10H, 10.0MM SHILEY CUFFED TRACH CAN; 10CN10R, 10.0MM ADT FLEX TRACH W TG CUFF; 10UN10A, 10.0MM UNCUFF TRACH TUBE X1;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1419-2023·2023-04-26
Beckman Coulter Free T3 Reagent Test Kit Recalled for Falsely Elevated Results
Beckman Coulter is recalling Access Free T3 reagent test kits (Catalog #A13422, Lot #233968) because approximately 15-20% of samples produce falsely elevated results that could lead to misdiagnosis and inappropriate thyroid treatment.
Product
Beckman Coulter Access Free T3, Triiodothyronine, Free, Catalog #A13422, each box contains 2 reagent packs.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1410-2023·2023-04-26
Medtronic INFINITY Spinal Fusion Screws Recalled for Material Defect
Medtronic is recalling 10 units of INFINITY Multi-Axial Screws distributed in the US and Canada because incorrect titanium material reduces gripping strength in affected lots.
Product
INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 32mm, REF 3604532; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1413-2023·2023-04-26
INFINITY Multi-Axial Spinal Screws Recalled for Titanium Material Defect
Medtronic is recalling INFINITY Multi-Axial Spinal Screws due to incorrect titanium material used in manufacturing, which reduces the gripping strength of the screw head. The affected screws are used for spinal fusion and stabilization.
Product
INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 34mm, REF 3604034; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1409-2023·2023-04-26
Spinal implant screws recalled due to defective titanium material
Medtronic is recalling 45 units of INFINITY Multi-Axial Screws (lot H5802983) worldwide because incorrect titanium was used, reducing the screw head's gripping strength. No illnesses or injuries have been reported.
Product
INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 24mm, REF 3604024; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1397-2023·2023-04-26
Habib EndoHPB Bipolar RF Catheter Recalled Due to Thermal Injury Risk
Boston Scientific recalls the Habib EndoHPB Bipolar RF Catheter used in pancreatic and biliary procedures due to inaccurate instructions that could result in excessive energy delivery and thermal injury.
Product
Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A radiofrequency (RF) catheter which provides bipolar energy to perform partial or complete ablation of tissue in the pancreatic and biliary tracts. UPN: M00500070
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1407-2023·2023-04-26
Surgical Centurion CirClamp Recalled for Incorrect Subassembly Size
Medline Industries is recalling 162 units of Centurion CirClamp surgical devices due to incorrect subassembly size. The defect could affect proper device function during surgical use.
Product
Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1394-2023·2023-04-26
Radiometer AQURE Software Recall Due to Patient Mix-up Risk
Radiometer is recalling AQURE laboratory software versions 2.5.2 through 2.6.1 due to a potential issue that could cause patient data mix-ups.
Product
AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage analytical devices and operator profiles. The user can associate patient data with test data. The system shows test results. The system receives data from co
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1399-2023·2023-04-26
Tobii Dynavox TD I-110 Speech Device Recalled Over Loose Battery Risk
The FDA is recalling the Tobii Dynavox TD I-110, a speech-generating device, because the battery may become loose from its housing and potentially be damaged. This affects users worldwide who depend on this device for communication.
Product
Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities. Catalog #: 750567
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1417-2023·2023-04-26
Philips 2D Perfusion Medical Imaging Software Recalled for Signal Processing Errors
Philips is recalling 2D Perfusion diagnostic imaging software due to signal processing errors that can produce inaccurate presentations, potentially affecting clinical decisions.
Product
2D Perfusion, release R1.0.x, R1.1.x, R1.2, and R1.2.1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1412-2023·2023-04-26
Spinal fixation screws recalled for reduced titanium gripping strength
Medtronic is recalling 90 INFINITY Multi-Axial Screws (Lot H5806345) due to incorrect titanium material that reduces screw head gripping strength. The defect affects 5 batches distributed in the US and Canada.
Product
INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 26mm, REF 3604026; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0733-2023·2023-04-26
Dietary Supplement with Unapproved COVID-19 Treatment Claims Recalled
Natural Solutions Foundation is recalling a colloidal silver dietary supplement labeled to treat COVID-19. The product violates FDA regulations prohibiting disease claims on dietary supplements.
Product
Dr. Rima Recommends The Silver Solution Immune System Support Dietary Supplement Nano Silver 10 ppm 16 fl. oz. (473 ml)
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1418-2023·2023-04-26
Olympus Single-Use Endoscopic Clip Fixing Device Recalled for Deployment Failure
Olympus is recalling single-use rotatable clip fixing devices used in endoscopy procedures. The clips may fail to deploy from the tube sheath during use.
Product
Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip Model HX 201UR 135 - Rotatable, 230 cm long, 2.8 scope channel, standard clip Model HX 201UR 135L - Rotatable, 230 cm long, 2.8 mm scope channel, Long clip
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1393-2023·2023-04-26
Smith & Nephew Knee Implant Component Mispack: Wrong Size Distributed
Smith & Nephew is recalling 12 JOURNEY II UNI Tibia Insert components due to a manufacturing mispack. Some boxes incorrectly contain a different size component.
Product
JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0536-2023·2023-04-26
Verapamil Hydrochloride Extended-Release Tablets Recalled for Failed Dissolution Specifications
Amerisource Health Services LLC is recalling Verapamil Hydrochloride Extended-Release Tablets 180 mg due to failed dissolution specifications affecting lots 1008622 and 1010026 distributed nationwide.
Product
Verapamil Hydrochloride Extended-Release Tablets, USP, 180 mg, 100 Tablets (10 x 10) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-504-01; NDC Unit Dose: 60687-504-11, barcode (01) 003 60687 504 11 7.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1392-2023·2023-04-26
BioFire FilmArray GI Panel Recalled for Potential False Negative Results
BioFire Diagnostics is recalling FilmArray Gastrointestinal Panel test kits due to a manufacturing issue that may produce false negative results. Affected units may fail to detect gastrointestinal infections.
Product
FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems, REF: RFIT-ASY-0116, (30 pouches/kit)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1414-2023·2023-04-26
Samsung GM85 Digital X-ray Imaging System Arm Latch Failure
NeuroLogica Corporation recalls 935 Samsung GM85 digital X-ray systems due to a faulty arm latch in the column support that could allow the arm to fall, creating a risk of bodily injury.
Product
Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1416-2023·2023-04-26
Philips SmartPerfusion Cardiac Imaging Software Recalled for Signal Processing Errors
Philips recalls SmartPerfusion cardiac imaging software for technical issues in signal generation and processing that can produce inaccurate diagnostic output.
Product
SmartPerfusion, release R1.0, R1.1, R1.1.1, R1.1.5, R1.1.5.1 and R1.1.6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0539-2023·2023-04-26
Antipsychotic Drug Recalled for Failed Quality Control Test
Ascend Laboratories is recalling 135 bottles of Aripiprazole 20 mg tablets nationwide due to failure of spectroscopic identification testing, indicating the product may not meet established quality standards.
Product
ARIPIPRAZOLE — ARIPIPRAZOLE (ARIPIPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1395-2023·2023-04-26
Instrument Kit Drill Guides Have Incorrect Depth Range
GEO Instrument Kits for EPS Plates contain drill guides marked with an incorrect depth range (30mm-60mm instead of 10mm-40mm), which could affect surgical implant placement.
Product
GEO Instrument Kit for EPS Plate, REF: 70120001, part of the GEO FirstFUSE 1st MTP Joint Arthrodesis Plating System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1415-2023·2023-04-26
Laboratory diagnostic device software issue may delay clinical diagnosis
BD Kiestra InoqulA+ (software versions 5.1/5.1.1) fails to display plate information after processing in clinical laboratories, risking diagnostic delays or specimen recollection.
Product
BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software version 5.1 and 5.1.1 as part of the Icefall A platform. An in vitro diagnostic medical device intended to automate specimen processing according to user-defined procedures and protocols. Catalog (Ref) No. : 447213
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1411-2023·2023-04-26
Spinal Implant Screws Recalled for Defective Titanium Material
Medtronic is recalling INFINITY spinal implant screws manufactured with incorrect titanium material. The defect reduces the screw's gripping strength, risking implant performance in critical spinal fusion surgery.
Product
INFINITY Occipitocervical Upper Thoracic System, PARTIALLY THREADED MULTI AXIAL SCREW, Size: 4.0mm x 22mm, REF 360PT4022; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unctio
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1398-2023·2023-04-26
Pressure Therapy System Recalled for Unauthorized Deep Vein Thrombosis Prevention Claim
Compass Health Brands is recalling the REX Pressure Therapy System because the user manual incorrectly claims the device can prevent deep vein thrombosis, an indication for which the device was not FDA-cleared.
Product
REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. Models: DVTREX-U and DVTREX -L
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1408-2023·2023-04-26
Medtronic SenSight Extension Tunneler Kit: manufacturing defect prevents dual-extension passage
Medtronic recalled approximately 1414 SenSight Extension Tunneler Kits due to a manufacturing defect where dual carriers were machined on only one side, preventing use for passing two extensions simultaneously.
Product
Medtronic SenSight Extension Tunneler Kit, REF B31030; The Extension Tunneler Kit is used to assist in the tunneling and passage of extensions for deep brain stimulation
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1406-2023·2023-04-26
Avanos Ballard Oral Care Swabs recalled for incorrect expiration date labeling
Avanos Medical is recalling Ballard Oral Care Swabs (codes 12241, 12243, 12251) due to incorrect expiration date labeling. The recall affects 5,475 cases distributed worldwide.
Product
Avanos Ballard Oral Care Swab, Bulk Packed, Product Codes: a) 12241, b) 12243, c) 12251
Category
Medical Device
Distribution
Distributed nationwide