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. 1,806 recalls have been distributed to Idaho in the last 12 months.
Showing 30901–30920 of 48,215 recalls
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GalaSHAPE 3D Recalled by Tepha Incorporated Due to Endotoxin values from...
The Issue: Endotoxin values from testing of retains slightly exceeded the established...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g Recalled by Oculus Innovative...
The Issue: Firm became aware that professional samples of Ceramax are not meeting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCl 1% Recalled by Cantrell Drug Company Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 USP Units Added to 0.9% Sodium Chloride Recalled by Cantrell...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Chloride Recalled by Cantrell Drug Company Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 Recalled by...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate 2 Recalled by Cantrell Drug Company Due to Lack of...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium Recalled by Cantrell Drug Company Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate 1 Recalled by Cantrell Drug Company Due to Lack of...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 Recalled by...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCl 0.25% in 0.9% Sodium Chloride Recalled by Cantrell Drug...
The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.