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. 1,723 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,723 in last 12 months

Showing 4554145560 of 49,990 recalls

Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595202010 Articular Surface XLPE CR ART SURF 1 Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597201101 Femur CR POROUS FEM COMP SIZE AML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597001333 Femur CR PRC SURF HDN FEM CO-NID CML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595501201 Provisional CR-FLEX FEM PROV SZ B-L Recalled by Zimmer, Inc. Due...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597201333 Femur CR POR SURF HDN FEM CO-NID CML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: SV Elastomeric Infusion Device. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597502010 Provisional AC ART SURF PROV 12/PUR 10 Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Multirate Infusor Devices. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
DrugJune 7, 2013· Sagent Pharmaceuticals Inc

Recalled Item: VECURONIUM Bromide for Injection Recalled by Sagent Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: product was not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 6, 2013· Bergin Fruit And Nut Co Inc

Recalled Item: 604293 MEGA OMEGA MIX 12/8 OZ SQ TUB Recalled by Bergin Fruit And Nut Co Inc...

The Issue: Bergin Fruit and Nut Company is initiating a recall on a number of pistachio...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 6, 2013· Bergin Fruit And Nut Co Inc

Recalled Item: 600943 PISTACHIOS KERNELS RAW 8/11 OZ SQ TUB Recalled by Bergin Fruit And...

The Issue: Bergin Fruit and Nut Company is initiating a recall on a number of pistachio...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 6, 2013· Bergin Fruit And Nut Co Inc

Recalled Item: 600910 PISTACHIOS SPLITS RAW 30# Recalled by Bergin Fruit And Nut Co Inc Due...

The Issue: Bergin Fruit and Nut Company is initiating a recall on a number of pistachio...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 6, 2013· Bergin Fruit And Nut Co Inc

Recalled Item: 601180 LOW GLYCEMIC SNACK MIX 12/4 OZ BERGIN RED BAG Recalled by Bergin...

The Issue: Bergin Fruit and Nut Company is initiating a recall on a number of pistachio...

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

Class I — Serious Health HazardOngoing
Refund