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. 2,279 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,279 in last 12 months

Showing 4374143760 of 48,770 recalls

Medical DeviceAugust 28, 2013· Carefusion 2200 Inc

Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...

The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...

The Issue: When using systems operating with software versions VD10A/G during a RAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Zimmer, Inc.

Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...

The Issue: Based on a review of historic packaging validations, it was determined that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Extension Shims Extension shims are manufactured from grade 5...

The Issue: Fit variation among all lots of S-LIFT extension shims with corresponding...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Captia Syphilis-G Test Kit Product Usage: This is an enzyme Recalled by...

The Issue: Trinity Biotech recalled Trinity Biotech Captia Syphilis IgG kits due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· H & H Associates

Recalled Item: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H &...

The Issue: Medical device tubing used for endotracheal airway application may become...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2013· Bayer Healthcare Llc

Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...

The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

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

Class II — Potential Health HazardOngoing
FoodAugust 26, 2013· Irene's Bakery & Gourmet Kitchen, Inc.

Recalled Item: Irene's Black & White Cookies Recalled by Irene's Bakery & Gourmet Kitchen,...

The Issue: Undeclared whey powder (milk allergen) sub-ingredient of chocolate...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Dextrose 50% Preservative Free SDV Injection Solution Recalled by Leiter's...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Bevacizumab (Avastin) 2.5mg/0.1mL PF Inj. Recalled by Leiter's Pharmacy Due...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Lidocaine/Phenylephrine PF 1%/1.5% Injectible vials Recalled by Leiter's...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Hyaluron (hyaluronidase) 150 units/mL Preserved Solution Recalled by...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 26, 2013· Zimmer, Inc.

Recalled Item: Zimmer Title 2 Bone Screw Remover Instrument Recalled by Zimmer, Inc. Due to...

The Issue: Possibility of the weld to the quick-connect breaking when force is applied...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Biomet 3i, LLC

Recalled Item: Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens...

The Issue: Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Snug Seat Inc

Recalled Item: Crocodile (size 3) are two-armed Recalled by Snug Seat Inc Due to The bolts,...

The Issue: The bolts, which secure the handles, on the Crocodile (size 3) could break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2013· Medtronic Xomed, Inc.

Recalled Item: Universal Titanium Prosthesis Recalled by Medtronic Xomed, Inc. Due to One...

The Issue: One lot of the product was assembled using the Cam Head version of the same...

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

Class II — Potential Health HazardOngoing