Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,436 recalls have been distributed to Idaho in the last 12 months.
Showing 19461–19480 of 27,833 recalls
Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code:...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 28CM Item Code: E278228 The...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode 28cm Item Code: E278428 The...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 45CM Item Code: E277345 The...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Blade Electrodes 28CM...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277236 The...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code:...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamond Coated Tips and Burs are accessories to the air Recalled by...
The Issue: Through an error, the labeling failed to include the symbol or other text...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamond Coated Tips and Burs are accessories to the air Recalled by...
The Issue: Through an error, the labeling failed to include the symbol or other text...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products...
The Issue: Several customer complaints about amplification performance issues when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TM Ardis Interbody System implant is a convex Recalled by Zimmer...
The Issue: This field action is being initiated following the firm's discovery of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego Recalled by Siemens Medical Solutions USA, Inc Due to Due...
The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is...
The Issue: Arrow is recalling due to incorrect labeling of products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies ( DCPS )
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...
The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPHERICAL HEAD (R) 6.5 MM CANCELLOUS SCREW Recalled by Smith & Nephew, Inc....
The Issue: The labels correctly state that the product should be a 25mm screw, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle Mixed Product Part Recalled...
The Issue: May contain two trocar tip stylets with coaxials or two blunt tip stylets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...
The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...
The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.