Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 4028140300 of 46,762 recalls

DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not CAPSULES 4X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not OINTMENT 3X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Ex PORTABLE SIPS 5X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Novartis Pharmaceuticals Corp.

Recalled Item: Ritalin HCl (methylphenidate HCl) USP Recalled by Novartis Pharmaceuticals...

The Issue: Labeling: Incorrect or Missing Package Insert; The back of the Medication...

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

Class III — Low RiskOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Fort TABLETS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo-Fort DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Fort CAPSULES 4X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Fort SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not TABLETS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· McKesson Packaging Services

Recalled Item: Venlafaxine Hydrochloride Recalled by McKesson Packaging Services Due to...

The Issue: Failed Dissolution Specification: Out of Specification dissolution results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
FoodFebruary 28, 2014· Unilever United States, Inc.

Recalled Item: Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs...

The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer Recalled by Roche...

The Issue: electrode used beyond the guaranteed in-use 52 week lifetime,may leak and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Teleflex Medical

Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...

The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...

The Issue: GE Healthcare has recently become aware of potential safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing