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. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 28721–28740 of 29,093 recalls
Recalled Item: I-STAT PT/INR cartridge Abbott Point of Care Inc. Abbott Park Recalled by...
The Issue: The i-STAT PT/INR cartridges have the potential to exhibit incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza. Radiological image processing system Recalled by...
The Issue: Siemens became aware of a potential malfunction when using syngo.plaza with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-01...
The Issue: Braemar has recently became aware of a battery related incident that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN...
The Issue: Some combinations of Calibrator lots and AlA PACKS resulted in Calibrator #6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System Console. Model: TX1 TX1 Tissue Removal Recalled by...
The Issue: Two reasons for recall. 1. Incorrect pressure relief valve installed inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultra-Short Magnetic Resonance Imaging System Recalled by Toshiba...
The Issue: The firm recalled due to a potentail problem with the position of the hold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The brand name of the device is AlgiNot Recalled by Kerr Corporation Due to...
The Issue: The firm recalled the product because it may cure harder than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus Tibia Plateau (component of the Columbus REVISION Knee System)...
The Issue: During an internal quality inspection, the tibia plateau was found to be out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW-I Anesthesia System The system is intended for use in Recalled by...
The Issue: A technical alarm may be generated on the FLOW-i system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow IV Fluid Warmer (510k name: EFLOW IV FLUID WARMER Recalled by Vital...
The Issue: The EnFlow Warmer Strap does not meet the requirements of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module with v2.0 software used Recalled...
The Issue: GE Healthcare became aware of two issues with the Patient Data Module using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle Recalled by...
The Issue: A Discrepancy was found on Hitachi AST (HA7 61) package insert. Limitations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Advansys Medial Lisfranc Plate (MLP) Recalled by Integra...
The Issue: Incorrect technique applied may cause potential rupture of the tibialis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The finger cots are made out of natural rubber. They Recalled by Afassco Inc...
The Issue: The firm is initiating a field correction because the product(s) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.