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. 2,618 recalls have been distributed to Iowa in the last 12 months.
Showing 10201–10220 of 49,990 recalls
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Large component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Medium component of VS Newborn Recalled by SUREPULSE...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Small component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Extra Small component of VS Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Extra Large component of VS Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clobetasol propionate Cream USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug: Low assay result observed during long-term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SenSight Connector Plug Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic is requesting return of a small number of units of the SenSight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of...
The Issue: Screw connection between the turbine head and the push button may loosen and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) Recalled by...
The Issue: Undeclared FD&C Yellow No. 5
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America Due...
The Issue: The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprint 200 wheeled stretcher Recalled by Linet Spol. S.r.o. Due to Labeling...
The Issue: Labeling being updated to assure user is securing the siderail to a locked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v Recalled by Urban...
The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v) Recalled by Urban Electric...
The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...
The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...
The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) # 9305 Recalled...
The Issue: Due to the detection of oil toxicity in several lots of Oil for Embryo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D...
The Issue: C-Arm unexpected movement may cause blunt trauma should the tube arm impinge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph mCT: a) Flow 64-4R Seismic Recalled by Siemens Medical...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.