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. 2,409 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,409 in last 12 months

Showing 3750137520 of 49,990 recalls

DrugJune 30, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...

The Issue: Crystallization; identified as calcium salt of Ketorolac

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2015· Mylan Pharmaceuticals Inc

Recalled Item: Capecitabine Tablets Recalled by Mylan Pharmaceuticals Inc Due to Failed...

The Issue: Failed Dissolution Specifications: low out-of-specification (OOS) results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...

The Issue: Crystallization; identified as calcium salt of Ketorolac

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 29, 2015· Merit Medical Systems, Inc.

Recalled Item: ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Becton Dickinson & Co.

Recalled Item: Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to The...

The Issue: The affected expired lots of product may have exhibited breakthrough growth...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Becton Dickinson & Co.

Recalled Item: Enterococcus Screen Agar QUAD Plate Recalled by Becton Dickinson & Co. Due...

The Issue: The affected expired lots of product may have exhibited breakthrough growth...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter HomeChoice and HomeChoice Pro APD systems Recalled by Baxter...

The Issue: Loud operating sounds, which was unacceptable to the end users when the...

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

Class III — Low RiskOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or Recalled by...

The Issue: When using the CIVCO biopsy attachments in combination with the ACUSON S...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
DrugJune 29, 2015· Qualitest Pharmaceuticals

Recalled Item: HydrOXYzine Hydrochloride Tablets Recalled by Qualitest Pharmaceuticals Due...

The Issue: Failed Tablet/Capsule Specifications; The identification codes on some...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2015· American Health Packaging

Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...

The Issue: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2015· Ranbaxy Inc.

Recalled Item: Absorica (isotretinoin) Capsules Recalled by Ranbaxy Inc. Due to Undeclared...

The Issue: Incorrect/Undeclared Excipients: Product contains undeclared FD&C Yellow No....

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 26, 2015· Vitamin Cottage Natural Food Markets, Inc.

Recalled Item: Natural Grocers Caribbean Fruit & Nut Mix Recalled by Vitamin Cottage...

The Issue: Vitamin Cottage Natural Food Markets, Inc is recalling one lot of Natural...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics VRE Broth Recalled by Hardy Diagnostics Due to Hardy...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Agar with VGA container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics MDR Acinetobacter container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing