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. 2,475 recalls have been distributed to Iowa in the last 12 months.
Showing 21261–21280 of 28,127 recalls
Recalled Item: EDI BZO UNCUT SHEET-CARD Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugCheck Pipette 10 Drug Test Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Clia Waived 12 panel Tilt Cup Recalled by Ameditech Inc Due to...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU) Recalled by...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC Recalled by Ameditech Inc Due to...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 10 Drug Panel Cassette Test Recalled by Ameditech Inc Due to...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immutest 10 Pnl Drug Screen Cup w/ Adult Recalled by Ameditech Inc Due to...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLAIR Endovascular Stent Graft Recalled by Bard Peripheral Vascular Inc Due...
The Issue: Bard Peripheral Vascular (BPV) is recalling the Bard Flair Endovascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The system provides the ability to transmit patient data files for storage...
The Issue: Display of SpO2 and Non-Invasive Blood Pressure (NIBP) Measurements May Freeze
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myelo-Nate CSF Sampling Kit Recalled by Utah Medical Products, Inc Due to...
The Issue: Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit...
The Issue: Possibility that the catheter peel-away component hub tabs may prematurely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...
The Issue: Complaint investigation concluded that although product quality requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SilverStat Recalled by TZ Medical Inc. Due to During a review of the IFU of...
The Issue: During a review of the IFU of the SilverStat Pads, it was found that the IFU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.