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. 987 recalls have been distributed to Alaska in the last 12 months.
Showing 18981–19000 of 46,762 recalls
Recalled Item: Revaclear Capillary Dialyzer 300 Recalled by Baxter Healthcare Corporation...
The Issue: There is the potential presence of particular matter in the header caps of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PneumoDart Recalled by Tytek Medical Inc Due to A defect involving an...
The Issue: A defect involving an occluded needle was discovered during a training exercise.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...
The Issue: Labeling mix-up - Indications on product label are incorrect.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...
The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T....
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion...
The Issue: Sterile barrier system may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranitidine Oral Solution Recalled by Precision Dose Inc. Due to CGMP...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Silver Bullet Recalled by Natures Rx Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eleganza 5 (AC powered adjustable bed) Recalled by Linet Spol. S.r.o. Due to...
The Issue: A component used within the side rail mechanism may malfunction, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with...
The Issue: Nonfunctional key due to the potential for damage to the key pins cause by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fentaNYL 500 mcg/250 mL (2 mcg/mL) Bupivacaine HCl 0.1% 250 Recalled by QuVa...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 1000 mcg/20 mL (50 mcg/mL) 20 mL in 20 mL Syringe Preservative Free...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.