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. 2,567 recalls have been distributed to Idaho in the last 12 months.
Showing 11461–11480 of 48,215 recalls
Recalled Item: DeRoyal limb holders: (1) DeRoyal Limb Holder Recalled by DeRoyal Industries...
The Issue: The webbing strap was laced improperly through the teeth of the buckle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) GE Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Inaccurate Distance and Area measurements with use of Global Stack viewport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Difluprednate Ophthalmic Emulsion Recalled by CIPLA Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: customer complaint for defective container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips EPIQ Ultrasound Systems (various models) used in conjunction with...
The Issue: Retroactive: Ultrasound may experience an unexpected automatic reboot,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Exacta-Mix 2400 compounding system Recalled by Baxter Healthcare...
The Issue: There is a potential for leaking valves on ports 1 to 4 in certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to SARS-CoV-2...
The Issue: SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e801 Immunoassay Analyzer Recalled by Roche Diagnostics Operations,...
The Issue: Software issue resulting in signals and sample test results of Pre-Wash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Dr....
The Issue: FAILED DISSOLUTION SPECIFICATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Dr....
The Issue: FAILED DISSOLUTION SPECIFICATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Pfizer Inc. Due to Presence of...
The Issue: Presence of particulate matter: particulate identified as a beetle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ready Meals Crab & Shrimp w/Ccktl SCE NET WT 12 Recalled by Albertsons...
The Issue: Undeclared allergens; fish, shellfish, egg, wheat, and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT Recalled by...
The Issue: Undeclared allergens; fish, shellfish, egg, and wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT Recalled by...
The Issue: Undeclared allergens; fish and shellfish
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kingdom Honey Royal Honey VIP The Ultimate Power Source Recalled by...
The Issue: Undeclared Sildenafil
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grappler Suture Anchor Recalled by Paragon 28, Inc. Due to Suture anchor may...
The Issue: Suture anchor may break upon insertion, which could lead to potential debris...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProPlan CMF Anatomical Model Recalled by Materialise USA LLC Due to...
The Issue: MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...
The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.