State
72,907 recalls have nationwide distribution and so reach Michigan. 9,517 additional recalls listed Michigan specifically in their distribution scope.
Of the 9,517 recalls naming Michigan we have scored against our rubric, 1,556 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,144 (23%) are Severe.
Which agencies issued them
These figures cover only the 9,517 recalls whose distribution notice names Michigan specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Plum Duo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Medartis APTUS 5.0 headed cannulated compression screws for bone fixation are being recalled because the cannulation of the screw is not centered. 13 units are affected.
MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.
An EXENT Analyser is being recalled after plates 2 and 3 were marked as passed although quality control appeared not to have been performed, despite samples being measured.
Plum Duo Infusion Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.
CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Dragonfly Thai Ginger Powder, 4.37 oz, packed for U.S. Trading Company, is being recalled over potential contamination with lead. 1,800 units are affected.
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
Bicarby Dialysate across six model numbers is being recalled because luer-lock leaks during preparation present a potential slip and fall hazard from fluid on the floor.
CORFLO Safety PEG Kits, catalog number 30-6316, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 41 kits are affected.
Halyard Pain Packs, kit code AMPK48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 120 kits affected.
Zep Alcohol Sanitizer Spray, ethanol 70%, in 55-gallon drums is being recalled for microbial contamination. Five drums are affected.
Allia IGS 3 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Nine units affected.
Halyard Towel Six Packs, kit code AMTS70-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 224 kits affected.
MIC Safety PEG Kits with ENFit Connectors, 24 Fr PUSH OTW, catalog number 8170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
CGuard Prime Carotid Stent Systems, 135 cm with a 9 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
Mahurkar Elite PASS Trays are being recalled because the Tegaderm CHG dressing specified in the product labeling was missing from certain lots. 25,627 units are affected.
Boston Scientific CSK stainless steel electrodes across several lengths are being recalled because the reusable electrodes may not meet expected performance levels. 31,923 units affected.
Boston Scientific TCN nitinol electrodes across four lengths are being recalled because the reusable electrodes may not meet expected performance levels. 49,251 units affected.
The SporeTraq Mail-In Spore Testing Service, 52 tests, is being recalled because an incorrect incubation process was performed on the product. 2,210 units are affected.
EXCOR Pediatric VAD System blood pump PU valves are being recalled because the inner package expiration date does not match the correct outer package date.
Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, are being recalled after an out-of-specification dissolution result at the ninth month of testing. 360 bottles affected.
Primidone Tablets, USP, 50 mg, from Amneal are being recalled over the potential for cross-contamination with acemetacin API due to an issue at the API manufacturer. 27,936 bottles affected.