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All product recalls affecting Maryland.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Maryland in the distribution area.
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
Ford Motor Company (Ford) is recalling certain 2025 Bronco Sport, Escape, and Lincoln Corsair vehicles. The Instrument Panel Cluster (IPC) may not illuminate at startup or while driving. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 101, "Control and Displays" and 102, "Transmission shift lever sequence, starter interlock, and transmission braking effect" as well as FMVSS numbers 126, 108, 135, 138, 208, and 305.
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
Defective delivery system - patches could be multi-stacked, adhered one on top of the other, in a single product pouch.
Use of embolization device with diameters greater-than-or-equal-to 4mm may lead to incomplete wall apposition and/or braid deformation (fish-mouthing/braid narrowing/braid collapse) noted during procedure and post-procedure, typically noted at 6-12 month imaging follow-up, potentially can lead to thrombosis and/or serious adverse events. Higher risk in females less-than-or-equal-to 45 years of age
Jayco, Inc. (Jayco) is recalling certain 2025 Jayco Jay Feather Micro trailers equipped with InVision Three Burner Cooktops. The aluminum burner tube may crack and cause a gas leak.
Autocar, LLC (Autocar) is recalling certain 2023-2025 E-ACTT vehicles. A software error may allow the vehicle to rollaway while on an incline and cause an engine stall.
Telcare, LLC has received customer complaints related to battery expansion/swelling for its Philips Connected Blood Glucose Meter (i.e., BGM 4 brand name) Monitoring System.. The issue was identified by post market surveillance data (customer complaints) - events of battery expansion/swelling and associated symptoms, e.g., leading to the device's removable back cover (battery port) to separate. If there is a loss of primary function of the device due to the described device defect, an immediate health consequence that may result is prolonged hypoglycemia or hyperglycemia due to delay in treatment, as the blood glucose measurement is not available to guide treatment. In a worst-case situation, there is potential for battery swelling to result in explosion of the battery and/ or device. Exposure to explosion, and subsequently projectiles from the explosion, may result in several immediate health consequences, including concussion, headache, dizziness, eye irritation, blurred vision, eye injury, and vision impairment.
Brinkley RV (Brinkley) is recalling certain 2024-2025 Model G fifth wheel trailers. The solar charge controller may fail and overheat.
This recall involves certain Cabinet Health 4 oz. Refillable Medicine Bottles with ABS plastic lids. The bottles are made of clear glass with blue, turquoise, orange or purple plastic lids labeled \"CABINET.\" Cabinet Health sold the bottles filled with over-the-counter drugs or as empty 4 oz. bottles. The recalled empty 4 oz. bottles were sold via cabinethealth.com from March 2023 through July 2024. Consumers with recalled empty bottles can identify them by the date of purchase. The recalled bottles filled with over-the-counter drugs have the following date codes on a sticker on the bottom of the bottle. Medication Name Lid Color Date Codes Tension Headache - Refillable Glass Bottle (Acetaminophen 500mg Caffeine 65mg) - 100 Count Blue 2029J07223 2029J07623 2029J07723 Allergy Relief - Refillable Glass Bottle (Diphenhydramine HCl 25mg) - 120 Count Turquoise 2265J07323 Pain Reliever and Nighttime Sleep Aid - Refillable Glass Bottle (Acetaminophen 500mg, Diphenhydramine 25mg) - 120 Count Blue 2127J06823 2127J23323 3040J23323 3051J23323 3051J23423Pain Reliever and Fever Reducer - Refillable Glass Bottle (Acetaminophen 500mg) - 120 Count Blue 2286J06323 2286J06523 2286J06623 2287J06623 2287J06723 Cough Relief - Refillable Glass Bottle (Dextromethorphan Hbr 15mg) - 60 Count Orange 2010J06923 2010J07023 3004J29623 3010J29623 3025J29623 Sleep Aid - Refillable Glass Bottle (Diphenhydramine HCl 50mg) - 70 Count Purple 3021J06823 3021J06923 3034J23423 3034J23523
This recall involves certain Matrix-brand Training Cycles models CXP-03, CXC-02, CXM-03, CXV and CXM-02. The recalled products have adjustable saddles and handlebars with an aluminum rear flywheel and a magnetic resistance system. They have matte black steel frames, forged steel cranks, dual-sided SPD pedals, four leveling feet and two transport wheels. "Matrix" is printed on the side. The model and serial numbers are located on a label on the lower rear area of the cycle frame. Recalled cycles have a serial number that contains a serial prefix of FC32, ZFC32B, FC33, FC36, FC29D or FC27. Model (Serial Prefix) Example Serial Numbers CXC-02 (FC32) FC32210900001 CXC-02 (ZFC32) ZFC32B240600001 CXM-02 (FC33) FC33210800001 CXM-03 (FC36) FC36240300001 CXP-03 (FC29) FC29D240600001 CXV (FC27) FC27210700001
This recall involves Pearhead Learning Sets with model number 87150. The Learning Sets are sold in a box with the words "learning set developmental toys for babies 0-6 months." The eight-piece Learning Sets include a cow stroller toy, crinkle sheep toy, black and white tummy time book with flashcards, plush activity cube and a wooden egg shaker rattle. The model number is printed on the side of the package under the bar code.
This recall involves the AMX Global Portable Folding Stadium Seat sold under the BJ's Wholesale or Black Sierra brand. The BJ's units have the "Berkley Jensen" logo on the back top side. The Black Sierra units have a Black Sierra Equipment logo on the top, right front side. The stadium seats fold down to a compact size of about 4 inches by 20 inches by 19 inches from the open size of 16 inches by 20 inches by 19 inches. They have a padded handle and shoulder strap. Recalled Berkley Jensen seats have the date code "04/2022" on the white tag on the bottom of the seat. Recalled Black Sierra Equipment seats have the date codes "05/2022" or "11/2022" on the white tag on the bottom of the seat. Only those date codes are included in this recall.