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 3282132840 of 48,770 recalls

FoodMay 5, 2016· Creative Snacks Co., LLC

Recalled Item: Creative Snacks Brain Food Recalled by Creative Snacks Co., LLC Due to...

The Issue: Potential presence of Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 5, 2016· Simply Delicious Inc.

Recalled Item: Bobo's Oat Bars Recalled by Simply Delicious Inc. Due to Simply Delicious is...

The Issue: Simply Delicious is recalling Lemon Poppyseed bars because they were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker PowerPRO (XT Recalled by Stryker Medical Division of Stryker...

The Issue: Complaints of smoke coming from the foot end of the cot. This reportedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Recalled...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Hickory Harvest FOODS Rucker's Cajun Mix 25 lb. bag in Recalled by Ohio...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Hickory Harvest FOODS Sweet & Salty Trail Mix 25 lb. Recalled by Ohio...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Big Y cranberry nut trail mix in plastic tub NET Recalled by Ohio Hickory...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Roasted & Salted Sunflower Kernels under the following brand names: Recalled...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Club Chef Raisin Sunflower Mix 4.8 oz bag Recalled by Ohio Hickory Harvest...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Roasted No Salt Sunflower Kernel s under the following brand Recalled by...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· NatureBox, Inc.

Recalled Item: Dark Cocoa Nom Noms 4.5oz. (128g) Recalled by NatureBox, Inc. Due to Firm...

The Issue: Firm was notified by third party warehouse that some Peanut Butter Nom Nom...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Brown & Haley Inc.

Recalled Item: Mountain Thins Trail Mix flavor Recalled by Brown & Haley Inc. Due to...

The Issue: Mountain Thins Trail Mix flavor, net wt. 5.3 oz., is recalled because it...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: VersaFx Femoral Fixation System Hex head compression screw 4.7 mm Recalled...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Manufacturing B.V....

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing