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.

52,535 total recalls
2,716 in last 12 months

Showing 2078120800 of 29,093 recalls

Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: 00720504022 ACETAB.CUPW/SH Recalled by Zimmer Trabecular Metal Technology,...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Covidien LLC

Recalled Item: Given Imaging Bravo¿ pH capsule delivery device Recalled by Covidien LLC Due...

The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Neff DAgostino Percutaneous Access Set Accessories Recalled by Cook Inc. Due...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· B. Braun Medical, Inc.

Recalled Item: Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage:...

The Issue: BBMI recently identified a potential for a tear in the outer blister...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Siemens Medical Solutions USA, Inc

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

The Issue: Siemens has identified changes in default carry forward workflow using...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Biosense Webster, Inc.

Recalled Item: Pentaray NAV High-Density Mapping Catheter Recalled by Biosense Webster,...

The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Toshiba American Medical Systems Inc

Recalled Item: MEXL-3010/A5- Vantage Titan 3T Magnetic Resonance Imaging System Product...

The Issue: A potential problem associated to the gradient coil (ASGC) in the Titan 3T...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Randox Laboratories, Limited

Recalled Item: Magnesium on RX Imola analyser IVD Recalled by Randox Laboratories, Limited...

The Issue: According to the firm, Carry over was observed when the amylase or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· B. Braun Medical, Inc.

Recalled Item: Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite...

The Issue: BBMI recently identified a potential for a tear in the outer blister...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Biosense Webster, Inc.

Recalled Item: Pentaray NAV High-Density Mapping ECO Catheter Recalled by Biosense Webster,...

The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2016· Beckman Coulter Inc.

Recalled Item: Lipase Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2016· Beckman Coulter Inc.

Recalled Item: Cholesterol Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2016· Beckman Coulter Inc.

Recalled Item: Lactate Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...

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

Class II — Potential Health HazardOngoing