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 21101–21120 of 29,093 recalls
Recalled Item: Curity All Purpose Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOPAZ MicroDebrider 0.8 mm Recalled by ArthroCare Corporation Due to During...
The Issue: During functional testing of devices after real time aging, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Gauze Sponges Recalled by Covidien LLC Due to Compromised sterility...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...
The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition: Intended to produce cross-sectional images of...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is Recalled by GE...
The Issue: Ferrous material in the SIGNA Pioneer Table Control Box (TCB) could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERION Unit (Vision Planner) Product Usage: The VERION Image Recalled by...
The Issue: Alcon is conducting a voluntary medical device correction of all VERION...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medica ISE Module Calibrant A Recalled by AMS Diagnostics, LLC Due to Lot...
The Issue: Lot was not functioning properly and not exhibiting the correct physical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.