Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1940119420 of 53,342 recalls

Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· BIOSENSE WEBSTER

Recalled Item: PENTARAY NAV eco HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx Recalled...

The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· BIOSENSE WEBSTER

Recalled Item: PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only Recalled...

The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 -...

The Issue: If the C-arm leaves its intended travel path due to a fault within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· LABORIE MEDICAL TECHNOLOGIES, CANADA ULC

Recalled Item: Pump Tube Set for MMS Libra and Solar Systems - Recalled by LABORIE MEDICAL...

The Issue: This field correction is being initiated to address potentially damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product...

The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2020· Ion Beam Applications S.A.

Recalled Item: Proteus 235 The Proton Therapy System - Proteus 235 (brand Recalled by Ion...

The Issue: Signature from the user is necessary to proceed with specific actions in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2020· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay Recalled by...

The Issue: The increased level of RPR reactivity in the BioPlex 2200 Syphilis Total &...

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

Class II — Potential Health HazardOngoing
DrugApril 21, 2020· Sandoz, Inc

Recalled Item: Infuvite PEDiatric Pharmacy Recalled by Sandoz, Inc Due to Defective...

The Issue: Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Product...

The Issue: Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Fresenius Kabi USA, LLC

Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2020· Fresenius Kabi USA, LLC

Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 20, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Cios Spin VA30-mobile X-Ray system Recalled by Siemens Medical...

The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· ROi CPS LLC

Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....

The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: B-Hydroxybutyrate LiquiColor Recalled by Cardinal Health Inc. Due to Three...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing