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. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 2300123020 of 48,770 recalls

Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: AMIA Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic...

The Issue: Negative bias results when using VITROS VALP Reagent, GEN 25.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
DrugDecember 10, 2018· Gordon Laboratories

Recalled Item: Monsel's (Ferric Subsulfate) Solution Recalled by Gordon Laboratories Due to...

The Issue: Superpotent Drug: contains higher levels of Iron than labeled.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun V3 42 Xlc(160w)(10 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented Tibial Component Product Usage: Knee replacement...

The Issue: Product mix up

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement...

The Issue: Product mix up

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Soothe & Cool Protect Moisture Guard Skin Protectant (petrolatum 59%)...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Medline Remedy Essential Barrier Skin Protectant Ointment (petrolatum 59%)...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Hydrocortisone Cream 1% MS Anti itch Cream with Intensive Healing 2 oz tubes...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Absorica (Isotretinoin) Capsules 30 mg USP Recalled by Sun Pharmaceutical...

The Issue: Subpotent Drug: Isotretinoin content results were lower than the...

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2018· Threshold Enterprises Ltd

Recalled Item: Planetary Herbals Mullein Lung Complex Recalled by Threshold Enterprises Ltd...

The Issue: Recall of Mullein Lung Complex due to a labeling error which indicates the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number Recalled by...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing