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. 2,488 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,488 in last 12 months

Showing 2108121100 of 49,990 recalls

Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Copeland HA Resurfacing Head Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Compress Recalled by Zimmer Biomet, Inc. Due to Elevated levels of bacterial...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· AZIYO BIOLOGICS

Recalled Item: BioEnvelope Recalled by AZIYO BIOLOGICS Due to Possible suture brittleness...

The Issue: Possible suture brittleness or breakage along the Envelope seam before the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: BALL NOSE GUIDE WIRE 80CM Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Hip systems Recalled by Zimmer Biomet, Inc. Due to Elevated levels...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
FoodAugust 21, 2019· Seattle Gourmet Foods Inc.

Recalled Item: FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a...

The Issue: FungusAmongUs Shiitake Organic Mushrooms are recalled due to undeclared...

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

Class III — Low RiskOngoing
Refund
DrugAugust 21, 2019· Macleods Pharma Usa Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...

The Issue: Subpotent Drug: Out of specification result during stability study in...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 20, 2019· Repro-Med Systems, Inc.

Recalled Item: 20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product...

The Issue: Mislabeled needle lengths

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Camera Recalled by Intuitive Surgical, Inc. Due to Some cameras...

The Issue: Some cameras were found to have residual soil adhered to the tip of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...

The Issue: Discrepancy between the correct expiration dates on the individual pouches...

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

Class III — Low RiskOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing