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. 2,760 recalls have been distributed to Maryland in the last 12 months.
Showing 19281–19300 of 29,093 recalls
Recalled Item: D & C Kit Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...
The Issue: Firm received a complaint of the tip holder breaking during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Laparotomy Pack - NS Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Basic Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Tray Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Open Procedure Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Venous Kit Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Latex HCY REAGENT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: The firm confirmed a reduced once-opened and on-board stability for N Latex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...
The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The...
The Issue: Lima Proximal Bodies were inadvertently re-sterilized. The safety screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee Tibial Insert Recalled by Encore Medical, Lp Due to The...
The Issue: The Empowr PS Insert was reported as missing the impaction slot feature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GN200 Caiman HF generators Recalled by Aesculap Implant Systems LLC Due to...
The Issue: Generators may have a faulty component which could impact the proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) has identified that in a rare sequence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...
The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) VANTA¿ XRF...
The Issue: It was discovered under rare circumstances the LED warning light circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.