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. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 3020130220 of 48,770 recalls

Medical DeviceJanuary 30, 2017· Hidrex GmbH

Recalled Item: Hidrex USA DP450 Recalled by Hidrex GmbH Due to The device was reclassified...

The Issue: The device was reclassified from a class III device to a class II device and...

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

Class III — Low RiskOngoing
DrugJanuary 27, 2017· Pharmedium Services, LLC

Recalled Item: Buffered Lidocaine Recalled by Pharmedium Services, LLC Due to Labeling;...

The Issue: Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2017· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Mirtazapine Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablets...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 27, 2017· Falafel King Ent, Inc.

Recalled Item: Falafel King Tzatziki Sauce. 10 ounce. Plastic container Recalled by Falafel...

The Issue: Falafel King announced a recall for their Tzatziki Sauce due to undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg...

The Issue: After a receiving a customer complaint for incorrect labeling, BD has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2017· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage:...

The Issue: Maquet has received several complaints involving the VASOVIEW HEMOPRO...

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

Class II — Potential Health HazardOngoing
FoodJanuary 26, 2017· NSE Products, Inc.

Recalled Item: Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 Recalled...

The Issue: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 26, 2017· COVIDIEN MEDTRONIC

Recalled Item: Valleylab Laparoscopic Handset Recalled by COVIDIEN MEDTRONIC Due to...

The Issue: Customer reports of the device handset continuing to operate after release...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2017· Radiometer America Inc

Recalled Item: ABL90 Flex Model #: 393-090 Portable Recalled by Radiometer America Inc Due...

The Issue: Reports that the sample type "cord blood" has been changed into the two...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2017· Radiometer America Inc

Recalled Item: The ABL800 Model#:All Recalled by Radiometer America Inc Due to Reports that...

The Issue: Reports that the sample type "cord blood" has been changed into the two...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS HI and Mevatron M2/Primus Mid-Energy Recalled by Siemens Medical...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON M 6730/6740 (MEX) Accelerator Recalled by Siemens Medical Solutions...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON MD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Integra LifeSciences Corp.

Recalled Item: The UNI-CP System Recalled by Integra LifeSciences Corp. Due to The firm...

The Issue: The firm received one complaint from one non-US sales representative...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON KD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON M 6700 (MX) Accelerator Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Quidel Corporation

Recalled Item: Influenza Transport Swab Packages Recalled by Quidel Corporation Due to...

The Issue: Quidel Corporation is recalling Influenza Transport Swab Packages because it...

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

Class II — Potential Health HazardOngoing
DrugJanuary 24, 2017· Hospira Inc., A Pfizer Company

Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Hospira Inc., A Pfizer...

The Issue: Presence of Particulate Matter: A hair was found stuck to the stopper of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2017· Strata Skin Sciences, Inc.

Recalled Item: XTRAC Excimer Laser Recalled by Strata Skin Sciences, Inc. Due to When the...

The Issue: When the Liquid Guide ( LLG) is not used according to the operator manual,...

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

Class II — Potential Health HazardOngoing