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 25501–25520 of 28,127 recalls
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL Recalled by...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER Recalled by Ecolab Inc...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER Recalled by Ecolab Inc Due...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL Recalled by...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...
The Issue: Upgrade installation script is designed to overwrite the same pouch files in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...
The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...
The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...
The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator A. Cat. #04800735 Recalled by Siemens Healthcare...
The Issue: Calibrator A lot CA77 is under-recovering to the assigned target for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...
The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by...
The Issue: The firm initiated this recall of certain lots of Illico Ti Cannulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...
The Issue: The product was registered and distributed as a Class I medical device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...
The Issue: High inlet water pressure beyond specification and the solenoid valve does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.