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.
Showing 18181–18200 of 53,342 recalls
Recalled Item: AC/DC POWER SUPPLY for 7400 Recalled by ESAOTE S.P.A Due to The AC/DC...
The Issue: The AC/DC adapter (power supply) of the portable ultrasound systems listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine Transdermal System 5 mcg/hour Recalled by Teva Pharmaceuticals...
The Issue: Failed Stability Specifications: Below specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: B. Braun Introcan IV Safety Catheters Recalled by Braxton Medical...
The Issue: Recalled products do not have FDA approval for sale in the United States.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055 Recalled by Biomet, Inc....
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055 Recalled by...
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Regenerex Primary Taper Cap Item Number 141269 Recalled by Biomet,...
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1500 Flex Heat and Moisture Exchanger Recalled by AB ULAX Due to Firm has...
The Issue: Firm has received 6 complaints that the Heat Moisture Exchanger (HME)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050 Recalled by Biomet,...
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Itch Relief Recalled by Akorn, Inc. Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar...
The Issue: Zimmer Biomet is conducting a medical device recall for three lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pH-D Feminine Health Boric Acid Vaginal Suppositories Recalled by pH-D...
The Issue: Marketed without an Approved NDA/ANDA.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tim Campbell Farm flat parsley in wooden crate. Neither Net Recalled by Tim...
The Issue: product tested positive for Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper...
The Issue: Product potentially being packaged without a taper adapter or baseplate. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Red-E Tablet Recalled by The Protein Shoppe Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA: product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 42 IN (107 cm) Appx 5.0 ml Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 IN (13 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.