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. 2,787 recalls have been distributed to Maryland in the last 12 months.
Showing 16621–16640 of 29,093 recalls
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T2100 Micro flex Drive Treadmill Recalled by GE Medical Systems Ultrasound &...
The Issue: A performance issue with customer owned spare parts, T2100 Microflex drive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PR4100 Microplate Reader US Recalled by Bio-Rad Laboratories Inc Due to The...
The Issue: The connector of the power supply was capable of fitting other components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Long Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Focal Catheter Recalled by PENTAX of America Inc Due to The...
The Issue: The catheter alignment arrow printed onto the strain relief is not aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 with DEPMED HARDENING KIT 12NC: 453567400741 Recalled by...
The Issue: The patient support head holder could contact the back ISO shelter wall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR Surgical Suite Option Product The MR Surgical Option when Recalled by GE...
The Issue: There is a potential safety issue with the table transfer release of the MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351 Recalled by...
The Issue: The patient support head holder could contact the back ISO shelter wall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 P with DEPMED HARDENING KIT 12NC: 453567400741 Recalled by...
The Issue: The patient support head holder could contact the back ISO shelter wall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...
The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...
The Issue: There is a potential for debris in the hole on the superior lateral aspect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.