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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 2601–2620 of 27,254 recalls
Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJOR NEURO PACK-LF Convenience kit Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoLock Close Vial Spike The Chemolock Closed System Recalled by ICU...
The Issue: Due to finished goods incorrectly packaged and labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) - In-Vitro Recalled by Becton...
The Issue: BD identified through potency testing as part of a stability test request to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscissor Tip (Disposable) Recalled by Microline Surgical, Inc. Due to A...
The Issue: A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V.A.C. Ulta Therapy Unit & ULTDEV01 The 3M" Recalled by KCI USA, INC. Due to...
The Issue: Due to potential system error alarm and the inability to initiate therapy as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Interventional Coil 3.0T Recalled by Philips North America Llc Due...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CI Analyzer. Catalog Numbers: 10947347. Recalled by Siemens...
The Issue: Potential that the IMT Diluent volume remaining (% remaining) does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BYTE Aligner System BYTE All-Day Aligner System BYTE Recalled by Straight...
The Issue: Virtual-only clinical workflow utilized for dental aligners and impression...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Breast Coil 3.0T 7ch Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 16ch 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Diagnostic Coil 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 7ch 3.0T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST SENSE Breast Dx Coil Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 7ch 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 16ch 3.0T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.