Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,444 recalls have been distributed to Iowa in the last 12 months.
Showing 31361–31380 of 49,990 recalls
Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: The company received a customer complaint for the inability to calibrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cappuccino Snack Mix Lot code: 20161027 Recalled by Dutch Valley Food...
The Issue: As a result of an ingredient supplier recall, Dutch Valley is issuing a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starkey Spring Water Recalled by Starkey Water Due to 12 ppb of arsenic was...
The Issue: 12 ppb of arsenic was detected in water sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Total Knee System Vanguard Open Box Femoral Components Item...
The Issue: packaging of some femoral components was incorrectly labeled as either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...
The Issue: Potential performance issue on strain categorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterscotch Drops - MB 1000 [or 4000] Count Recalled by Blommer Chocolate...
The Issue: Possible contamination of product with Salmonella as product includes the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 70 Milk Confectionery Coating - MB Recalled by Blommer Chocolate Co., Inc....
The Issue: Possible contamination of product with Salmonella as product includes the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cocie High Protein 90 White Confectionery Discs - MB Recalled by Blommer...
The Issue: Possible contamination of product with Salmonella as product includes the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 34 White Confectionery Coating Recalled by Blommer Chocolate Co., Inc. Due...
The Issue: Possible contamination of product with Salmonella as product includes the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.