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. 2,417 recalls have been distributed to Alaska in the last 12 months.
Showing 19361–19380 of 46,762 recalls
Recalled Item: Viatrexx-Arthros Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Immunexx Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Ithurts Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Facial Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-MuSkel-Neural Recalled by 8046255 Canada Inc. DBA Viatrexx Due to...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Relief + Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Systemic Detox Recalled by 8046255 Canada Inc. DBA Viatrexx Due to...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Neuro Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Male+ Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Adipose Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail...
The Issue: Firm is recalling two lots of 2 lb. organic soybeans because they have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Levo Arm Label: LEVO ARM MIZUHO OSI Recalled by Mizuho OSI Due to Due to the...
The Issue: Due to the potential for fluid ingress into the Arm which could affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urine Electrolyte Diluent Recalled by Ortho Clinical Diagnostics Inc Due to...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7% BSA (Bovine Serum Albumin) Recalled by Ortho Clinical Diagnostics Inc Due...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiofrequency Grounding Pad Recalled by Abbott Medical Due to Affected lots...
The Issue: Affected lots were manufactured with the protective release liner in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levetiracetam Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert - the incorrect package insert...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.