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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 2981–3000 of 29,286 recalls
Recalled Item: SURG STRP 3X6 Model/Catalog Number: 801456. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/4X3 Model/Catalog Number: 801398. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG STRP 3-1/2X6 Model/Catalog Number:801457. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/2X1 Model/Catalog Number: 801402. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG STRP 1X6-200 Model/Catalog Number: 801453. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICR PATIE RND Model/Catalog Number: 801396. CODMAN Surgical Patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/4X1-1/2 Model/Catalog Number: 801397. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/2X3 Model/Catalog Number: 801407. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG STRP 1/4X6 Model/Catalog Number: 801450. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1X1 Model/Catalog Number: 801403. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...
The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...
The Issue: To better define the drying procedures described in the IFU to improve the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...
The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult Ear Clip SpO2 Sensor Recalled by Nihon Kohden America Inc...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor Recalled by...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...
The Issue: The beds have a potential for an interface issue with the Rauland Responder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...
The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.