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. 1,720 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,720 in last 12 months

Showing 4892148940 of 49,990 recalls

DrugJune 5, 2012· Watson Laboratories Inc

Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...

The Issue: Impurities/Degradation Products: High Out-of-specification results were...

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

Class III — Low RiskOngoing
Refund
DrugJune 5, 2012· Bristol-myers Squibb Company

Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...

The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 5, 2012· Campbell Soup Supply Co., LLC

Recalled Item: Campbell's Oyster Stew Recalled by Campbell Soup Supply Co., LLC Due to The...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2012· GlaxoSmithKline Inc

Recalled Item: Trizivir (abacavir sulfate 300mg Recalled by GlaxoSmithKline Inc Due to...

The Issue: Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg tables, Lot...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 4, 2012· Leica Microsystems, Inc.

Recalled Item: Leica M525 F50 Surgical Microscope Recalled by Leica Microsystems, Inc. Due...

The Issue: Leica Microsystems evaluated data showing that a malfunction resulting in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2012· Aesculap, Inc.

Recalled Item: Aesculap(R) - Miethke Shunt System Recalled by Aesculap, Inc. Due to The...

The Issue: The deflector may not move freely on the ventricular catheter. The deflector...

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

Class II — Potential Health HazardOngoing
FoodJune 4, 2012· Botanical Laboratories Inc

Recalled Item: Product is a liquid dietary supplement packaged in white plastic Recalled by...

The Issue: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4-Hytrel Zipper Toga Product Usage - The togas are intended Recalled by...

The Issue: The clear tape, that is intended to aid in the prevention of patients...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...

The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that the outer carton label of this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Advanced Sterilization Products

Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...

The Issue: The recall was initiated because Advanced Sterilization Products has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...

The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...

The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...

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

Class II — Potential Health HazardOngoing