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. 2,447 recalls have been distributed to Iowa in the last 12 months.
Showing 27301–27320 of 28,127 recalls
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stat-Check Resuscitator Recalled by Ventlab Corporation Due to Possible...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Adult Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Child Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR220amx Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR200amx. Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component...
The Issue: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromovision High Definition (HD) Wireless Camera Recalled by Berchtold...
The Issue: Defective camera: There is a possibility that the connection of the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTec Recalled by Sentec AG Due to SenTec is recalling a number of V-Sign"2...
The Issue: SenTec is recalling a number of V-Sign"2 Sensors due to a problem regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRISpec" CA/CB two-part urine chemistry control twin set Recalled by Iris...
The Issue: The firm recalled after it received complaints of IRISpec CA/CB two part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: Recalled...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finapres Medical Systems Portapres with NiMh battery pack Product Usage:...
The Issue: Battery may become hot and leak
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic...
The Issue: Baxter discovered that a Baxter technical service representative was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i Recalled by Beckman...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.