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. 966 recalls have been distributed to Idaho in the last 12 months.
Showing 35201–35220 of 48,215 recalls
Recalled Item: DA-2006P - Defibrillator / Pacer Analyzer Recalled by BC Group International...
The Issue: Device is not functioning as intended: Two wires running to the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rainbow Reusable Sensors. RAINBOW DCI-DC3 Recalled by Masimo Corporation Due...
The Issue: These sensors were manufactured with incompatible configurations. This could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250 Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube Recalled by Geritrex Corp Due...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbo-O-Philic 40 Cream 40% (Urea) tubes Recalled by Geritrex Corp Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IOL Master 5.5: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 500: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Injectable Implant 1.5cc Recalled by Merz North...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA)...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN Injectable Implant 1.0 cc Gel Recalled by Merz North America, Inc....
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cavity 8 Gauge Spine Wand indicated for resection Recalled by ArthroCare...
The Issue: There is cracking in the tray when the device is snapped into place. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meclizine Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meclizine Hydrochloride Tablets USP Recalled by Par Pharmaceutical Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: David Trail Mix Sweet & Salty individual plastic bags net Recalled by...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152...
The Issue: Medtronic has discovered that select lots of the Amphirion Deep PTA Balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon GranuFlo Dissolution Unit - P/N G047-80101. For...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units) Recalled...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.