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. 2,800 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,800 in last 12 months

Showing 1500115020 of 29,093 recalls

Medical DeviceDecember 12, 2018· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Product Usage: The Proton Therapy System - Proteus Recalled by...

The Issue: There is a risk of detachment of the Compact Gantry Rolling Floor.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: AMIA Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic...

The Issue: Negative bias results when using VITROS VALP Reagent, GEN 25.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun V3 42 Xlc(160w)(10 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented Tibial Component Product Usage: Knee replacement...

The Issue: Product mix up

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement...

The Issue: Product mix up

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number Recalled by...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK STEM with Microporous Surface MP Reconstruction Prosthesis Recalled by...

The Issue: The reaming guide and the guide rod can't be screwed into the intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE¿ PPH Hemorrhoidal Circular Stapler Product Code:PPH03 PPH03: The...

The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE¿ HCS Hemorrhoidal Circular Stapler Product Code: PPH01 PPH01: The...

The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2018· Carl Zeiss Meditec, Inc.

Recalled Item: VisuMax Software Version 2.10.13 with activated Software-Module ReLEx...

The Issue: VisuMax devices with software version 2.10.13 and activated SW-Module ReLEx...

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

Class II — Potential Health HazardOngoing