Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,663 recalls have been distributed to Maryland in the last 12 months.
Showing 31321–31340 of 52,535 recalls
Recalled Item: Nutri-Dyn Calcium D-Glucarate Plus Recalled by Nutri-Dyn Midwest, Inc. Due...
The Issue: During production of St. John's Wort, Lot 160876, a number of bottles were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chef Luca's Italian Gluten Free Foods Lasagna Al Forno Baked Cheese Lasagna...
The Issue: Product contains undeclared eggs
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....
The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kite Hill Mushroom and Ricotta Ravioli Recalled by Lyrical Foods Inc Due to...
The Issue: Ingredient statement for Lyrical Foods Mushroom and Ricotta Flavor Ravioli...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system Recalled by...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Creator Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo MR355 Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...
The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets...
The Issue: Product size listed on the labeling is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clear Flashback Needle 7cm x 18G AMC/4 Recalled by Argon Medical Devices,...
The Issue: Argon Medical has received a complaint from one of their distributors of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Install CD Recalled by Medtronic Navigation, Inc. Due to Software issue...
The Issue: Software issue related to the StealthStation S7 system and the Synergy Spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.