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. 1,840 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,840 in last 12 months

Showing 3002130040 of 49,990 recalls

Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugApril 27, 2017· Hetero USA Inc

Recalled Item: Acyclovir Tablets Recalled by Hetero USA Inc Due to Presence of Foreign...

The Issue: Presence of Foreign Substance: human hair melded into tablet.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 27, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol Transdermal System) 0.1 mg per day Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for peel force from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodApril 27, 2017· Lords Organics Llc

Recalled Item: Organic Veda brand Ginger Powder Recalled by Lords Organics Llc Due to...

The Issue: Lord Organics is recalling ginger powder because it has the potential to be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 26, 2017· Phoenix Food, LLC

Recalled Item: Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 Recalled by Phoenix Food,...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 26, 2017· Rich Products Corp

Recalled Item: ARTISAN CRUST PIZZA DOUGH 24/18 Recalled by Rich Products Corp Due to...

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2017· Rich Products Corp

Recalled Item: 7 OZ PIZZA DOUGH BALL Recalled by Rich Products Corp Due to Potential E....

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2017· Rich Products Corp

Recalled Item: ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and...

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 26, 2017· Iba Dosimetry

Recalled Item: Large Stealth Chamber Recalled by Iba Dosimetry Due to When the Stealth...

The Issue: When the Stealth Chamber is used as a detector in relative dosimetry,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2017· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffmann LRF Safety Clip (Bone Transport Strut) Recalled by Stryker...

The Issue: Stryker is recalling Hoffmann LRF (Limb Reconstruction Frame) System Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· BioMerieux SA

Recalled Item: ETEST ETP32 (Ertapenem) Ref. 531640 Recalled by BioMerieux SA Due to False...

The Issue: False susceptible results

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Bard Access Systems Inc.

Recalled Item: StatLock¿ IV Premium Catheter Stabilization Device Recalled by Bard Access...

The Issue: StatLockTM IV Premium Catheter Stabilization Device may contain an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing