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. 2,716 recalls have been distributed to Maryland in the last 12 months.
Showing 22201–22220 of 29,093 recalls
Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...
The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...
The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Element Press-Fit Recalled by Exactech, Inc. Due to Eight (8)...
The Issue: Eight (8) pieces did not receive the specified Hydroxyapatite (HA) coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Bone Marrow Biopsy Trays Catalogue No. 3404253 Various medical...
The Issue: Integra received an Urgent Drug Recall Notice from Hospira Inc. for their 1%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...
The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 100 system included the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Envoy 500 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 300 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sentinel MULTIGENT Ammonia Ultra Reagent Recalled by Sentinel CH SpA Due to...
The Issue: Results for ammonia are below the linear range of the assay for samples that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...
The Issue: Users can merge a device import file with an image study that already has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software with Issuer of Patient ID (IPID). The Recalled by...
The Issue: For sites using the Issuer of Patient ID (IPID), the system will display the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valeant Pharmaceuticals North America Recalled by Valeant Pharmacueticals...
The Issue: The Serial I.D. Label and some information in the Operation Manual for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is...
The Issue: One mislabeled dose of TheraSphere¿ Y-90 Glass Microspheres, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Duracon Flat Tibial Wedge Cemented use only Sterile....
The Issue: Stryker Orthopaedics has received two customer complaints regarding Duracon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Screw Inserter Recalled by Synthes (USA) Products LLC Due to Certain...
The Issue: Certain lots of the Screw Inserter may be etched with incorrect graphics....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Lightbox Recalled by Brainlab AG Due to Potentially incorrectly...
The Issue: Potentially incorrectly displayed objects when actively deselecting a fused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.