Product Recalls in Wisconsin
Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,616 recalls have been distributed to Wisconsin in the last 12 months.
Showing 17121–17140 of 28,744 recalls
Recalled Item: Alden HP59 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Xstar Safety Crescent Recalled by Beaver-Visitec International...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o Recalled by...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Xstar Safety Slit Knife: (a) Recalled by Beaver-Visitec...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASTERA Multifocal Toric Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...
The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver EdgeAhead Safety Knife Recalled by Beaver-Visitec International...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...
The Issue: The firm received reports of two breakages of the pin tips which occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE(TM) BRAND Recalled by 3M Company - Health Care Business Due to Mold was...
The Issue: Mold was found on the non-patient contact surfaces of the product and was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The internal...
The Issue: The internal configuration of the electrometers and the Real-Time control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to (1) Under...
The Issue: (1) Under certain conditions, if a malfunction alarm occurs while the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.