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. 1,035 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,035 in last 12 months

Showing 18681–18700 of 53,342 recalls

Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 12 IN(30cm) APPX 2.1ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 9.5 IN (24cm)APPX 1.1ml SMALLBORE TRIFUSE SET Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 8 IN (20CM) APPX 1.3ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: APPX 0.75ml Recalled by ICU Medical, Inc. Due to Identification of a...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7 IN (18CM) APPX 0.26ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: Appx 0.82 ml Recalled by ICU Medical, Inc. Due to Identification of a...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way Recalled by ICU Medical,...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 13 IN (33cm) APPX 0.96 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 13 IN(33cm) APPX 1.0 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx 0.35 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 114" (290 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 26 IN(66cm) APPX 3.9 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 10 IN (25cm) APPX 1.5ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: DISTALE - 203 cm (80") Bifuse Ext Set w/6 Gang 1o2 Manifold Recalled by ICU...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· OrthoPediatrics Corp

Recalled Item: Orthopedics 6.0MM ROD Recalled by OrthoPediatrics Corp Due to Product may...

The Issue: Product may have incorrect laser etched alignment lines, the non-conforming...

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

Class II — Potential Health HazardOngoing