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. 959 recalls have been distributed to Iowa in the last 12 months.
Showing 41881–41900 of 49,990 recalls
Recalled Item: Humidifier Adaptor Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMI Duro-Med Industries Rollator Transport Chair Recalled by Briggs Medical...
The Issue: There have been 5 customer reports of a 501-1018 series DMI Rollator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Recalled...
The Issue: There is a potential for a leak. A molding defect in the connector that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak SW/EAU Sterile Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak SW/EAU Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aqua 540 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the respiratory gas humidifier adaptor packaging may be creased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humidifier Adaptor 040 Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...
The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch Critical Care Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has received complaints from the field alleging instances where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a...
The Issue: In the case of a loss of GUI display due to a Backlight Inverter PCBA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ferrous Gluconate Tablets Recalled by National Vitamin Co Inc Due to Mislabeling
The Issue: National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROSA Surgical Device 2.5.8 It is intended to be used Recalled by Zimmer...
The Issue: Software corrections reactivating the cooperative endoscopy mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.