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. 1,000 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,000 in last 12 months

Showing 35381–35400 of 52,535 recalls

Medical DeviceJune 24, 2016· Cook Inc.

Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...

The Issue: Potential coating contamination with glass particles.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· Baxter Healthcare Corp.

Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...

The Issue: Baxter is issuing a safety alert in response to postmarketing reports...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· Moller Vital

Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...

The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 24, 2016· Teva North America

Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva North America Due to...

The Issue: Superpotent drug: Out of specification test result for assay during...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2016· Hospira Inc.

Recalled Item: Diazepam Injection USP 10mg/2mL (5 mg/mL Recalled by Hospira Inc. Due to...

The Issue: Crystallization: Product contains particulate identified to be crystallized...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: AUTOCOMP6 XP High Speed Compounder Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...

The Issue: Incorrect values for the volume calculation. Software update VB30B via...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Olympus Corporation of the Americas

Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...

The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...

The Issue: Varian Medical Systems has received reports that unintended changes were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: AUTOCOMP6 High Speed Compounder Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...

The Issue: Varian Medical Systems has received reports that unintended changes were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with...

The Issue: It was reported that the secondary locking mechanism, and its corresponding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Modular Handle Triathlon Instruments Recalled by...

The Issue: Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Edan Diagnostics

Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...

The Issue: Incorrect CO2 readings with some patient monitors.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Dual Chamber Container fill and transfer sets Recalled by The Metrix Company...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: AUTOCOMP6 XPS High Speed Compounder Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing