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. 2,245 recalls have been distributed to Alaska in the last 12 months.
Showing 46541–46560 of 46,762 recalls
Recalled Item: Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source Recalled by...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM Central Station Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a....
The Issue: There is a software anomaly with the DPM Central Monitoring System where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Catalog (part number 20-0020) utilized with the Electric and...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cutting Bur Chart (part number 20-0019) utilized with the Electric Recalled...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00...
The Issue: Braemar Inc., became aware of a battery related incident that occurred with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Recalled by...
The Issue: In Online Entry (OEx) there are two scenarios where a Test result from one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mrs. Bridges Scottish Raspberry Preserve ("Jam") Recalled by The TJX...
The Issue: The firm is initiating the recall for Scottish Raspberry Preserve due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IO Fix IntraOsseous Fixation System Recalled by Extremity Medical LLC Due to...
The Issue: Product Event Reports revealed that lag screw passes through washer (e.g....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metronidazole Tablets Recalled by Physicians Total Care, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Some tablets had the potential to not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xactdose Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to...
The Issue: Defective container; lidding deformity allows the contained product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Recalled by GE...
The Issue: GE Healthcare conducted a recall involving 2 events affecting the GE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.