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. 2,450 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,450 in last 12 months

Showing 1858118600 of 48,770 recalls

FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Mixed Greens 4 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Spring Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Red Clover 4 oz Recalled by Chicago Indoor Garden, Inc. Due to Potential E....

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T...

The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description:...

The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2020· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. Recalled by...

The Issue: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2020· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2020· Boddingtons Plastics Ltd

Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...

The Issue: Updated Instructions For Use- to contraindications and potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Skytron, Div. The KMW Group, Inc

Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...

The Issue: Intermittent failure of a signal being sent to a monitor from the touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...

The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...

The Issue: As part of an investigation into a biocompatibility test discrepancy where a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: AUTOLITH URO-TCH 9FR PROBE 54CM Recalled by Northgate Technologies, Inc. Due...

The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products TT4 Reagent Pack Recalled by Ortho Clinical...

The Issue: The specified reagent packs exhibit an increase in the frequency of...

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

Class III — Low RiskOngoing
Medical DeviceMarch 10, 2020· Radiometer Medical ApS

Recalled Item: ABL800 FLEX Recalled by Radiometer Medical ApS Due to Analyzer's barcode...

The Issue: Analyzer's barcode reader misinterprets the contents of barcode label used...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Sotalol HCL Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of particulate matter. presence of metal particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Sun Pharmaceutical Industries, Inc....

The Issue: Presence of foreign substance: Foreign matter has been identified as latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Bekyree (desogestrel and ethinyl estradiol tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class III — Low RiskOngoing
Refund
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars - Variety Pack (contains 24 x 5 oz. units) Strawberry...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars Pineapple Recalled by Dreyers Grand Ice Cream, Inc. Due...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

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

Class II — Potential Health HazardOngoing
Refund