Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,352 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,352 in last 12 months

Showing 3372133740 of 48,770 recalls

Medical DeviceMarch 1, 2016· GE Medical Systems, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2016· Alcon Research, Ltd.

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.

Class II — Potential Health HazardOngoing
DrugMarch 1, 2016· Sagent Pharmaceuticals Inc

Recalled Item: Fluconazole Injection Recalled by Sagent Pharmaceuticals Inc Due to Cross...

The Issue: Cross contamination with other products: metronidazole

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2016· Allegiant Health

Recalled Item: col-rite (docusate sodium) stool softener softgels Recalled by Allegiant...

The Issue: Superpotent Drug: High out of specification results for assay at the 6 month...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 29, 2016· AMS Diagnostics, LLC

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.

Class III — Low RiskOngoing
Medical DeviceFebruary 29, 2016· Karl Storz Endovision, Inc.

Recalled Item: ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use Recalled by...

The Issue: Endoscope cleaning brush 11276CL may not fit resulting in an inability to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· Richard Wolf Medical Instruments Corp.

Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...

The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· Cardinal Health

Recalled Item: Gomco Style Circumcision Clamp Trays is an instrument used to Recalled by...

The Issue: Two lots of Gomco Style Circumcision Clamp Trays, SSI-0034 and 10-1100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· Nidek Inc

Recalled Item: RT-5100 (Epic 5100) and RT 3100 : Product Usage: Recalled by Nidek Inc Due...

The Issue: There has been a reoccurrence of an issue on the RT 5100 and RT 3100 of the...

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

Class II — Potential Health HazardOngoing
FoodFebruary 29, 2016· Whole Foods Market

Recalled Item: Whole Foods Market Maytag Blue Cheese Recalled by Whole Foods Market Due to...

The Issue: Possible contamination with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 26, 2016· Rich Products Corp

Recalled Item: New York Style Chocolate Iced ¿clairs under the following labels: Recalled...

The Issue: Products were recalled due to the potential presence of plastic foreign...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 26, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...

The Issue: Dialyzer header leak due to possible improper torque

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...

The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...

The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2016· Torrent Pharmaceuticals Limited

Recalled Item: Telmisartan Tablets Recalled by Torrent Pharmaceuticals Limited Due to...

The Issue: Presence of Foreign Substance: Product complaint for the presence of foreign...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 24, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...

The Issue: After importing, the segmentation results appear mirrored at the CARTO...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Purewick Corporation

Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...

The Issue: PureWick is recalling external catheter for women Wicks because the labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ab Sciex

Recalled Item: Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the Recalled by Ab...

The Issue: Wrong quantitative results may be displayed in a report from the device,...

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

Class II — Potential Health HazardOngoing