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. 1,031 recalls have been distributed to Alaska in the last 12 months.
Showing 13801–13820 of 27,254 recalls
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...
The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...
The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: Recalled...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...
The Issue: A complaint trend was observed for post-operative loss of height and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MoniTorr INS1100 INS-1100 CSF Drainage System used with Pole Mount Recalled...
The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.