State

Michigan product recalls

20,305 recalls have nationwide distribution and so reach Michigan. 0 additional recalls listed Michigan specifically in their distribution scope.

About recalls in Michigan

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Michigan consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

12401–12425 of 20305

SevereFDA (Food)·F-1243-2023·2023-07-19
Multiple Brands of Dill Pickle Pretzels Recalled for Undeclared Milk
Dakota Style, Inc. is recalling multiple brands of dill pickle pretzels nationwide because they may contain undeclared milk, a major allergen. Consumers with milk allergies should not consume these products.
Product
1. Hy-Vee Dill Pickle Braided Pretzels, 10oz poly bags, UPC: UPC: 75450-24308, 12 pack; 2. Schnucks Dill Pickle Pretzel Schticks, 10oz poly bags, UPC: 41318-25268, 12 pack; 3. Best Choice Dill Pickle Pretzel Twists, 10oz poly bags, UPC: 700038-66480, 12 pack; 4. Gelson's Dill P
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1241-2023·2023-07-19
Pretzel products recalled for undeclared milk allergen nationwide
Dakota Style, Inc. is recalling salt and vinegar pretzel products nationwide because they may contain undeclared milk. Consumers with milk allergies should not consume these products.
Product
1. Hy-Vee Salt & Vinegar Braided Pretzels, 10 oz poly bags, UPC: UPC: 75450-27706, 12 pack; 2. Dakota Style Salt & Vinegar Pretzel Kravings, 4.5 oz poly bags, UPC: 84872-60030, 6 pack; 3. Dakota Style Salt & Vinegar Pretzel Kravings, 10 oz poly bags, UPC 84872-60018, 12 pack, 4
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2110-2023·2023-07-19
Abbott Cardiac Catheter Sheath Recalled Due to Air Embolism Risk
Abbott is recalling the Amplatzer Steerable Delivery Sheath (ASDS), a cardiac catheter, due to a 0.77% reported incidence rate of air embolism during procedures. The recalled 675 units are distributed worldwide.
Product
Abbott Amplatzer Steerable Delivery Sheath (ASDS), REF ASDS-14F-075, is a percutaneous catheter (cardiac).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2133-2023·2023-07-19
Medline Non-Sterile PVP Solution Kits Mislabeled as Sterile
Medline is recalling Total Knee Theda surgical kits where the non-sterile PVP solution was mislabeled as sterile. Healthcare providers should immediately stop using the recalled kits and contact Medline.
Product
MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: TOTAL KNEE THEDA, Model Number DYNJ908683A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0909-2023·2023-07-19
Allergy Relief Fexofenadine Tablets Recalled for Failed Impurity Specifications
L. Perrigo's Allergy Relief 180 mg tablets are being recalled due to failed impurity and degradation specifications. The recall affects 32,904 cartons distributed nationwide.
Product
ALLERGY RELIEF — ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2109-2023·2023-07-19
Surgical chest support device recalled for potential cracking at attachment
Baxter Healthcare recalls 1,010 Allen Advance Chest Support devices due to potential cracking where the support attaches to operating room table rails. No injuries reported.
Product
Allen Advance Chest Support with Pad
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2130-2023·2023-07-19
Ambulance stretcher base leg assembly may bend causing tip and unstable motion
Stryker Power-PRO 2 ambulance cots may develop bent base leg assemblies, risking cot tips, unstable motion, and operational difficulties. Approximately 1,980 units were recalled.
Product
Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a maximum weight of 700 lb (318 kg). Model Number: 6507
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0922-2023·2023-07-19
Artificial Tears Eye Drops Recalled Due to Manufacturing Facility Contamination
Delsam Pharma's artificial tears eye drops are being recalled nationwide due to confirmed contamination linked to manufacturing facility defects. All affected lots were distributed via two distributors.
Product
Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2121-2023·2023-07-19
Medtronic Catalyft LS Spinal Implant Recall Due to Out-of-Specification Geometry
Medtronic recalls 10 units of Catalyft LS spinal implants due to potential out-of-specification device geometries. The affected implants may not properly support or accommodate patient anatomy during lumbar fusion surgery.
Product
Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027722, spinal implant
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2117-2023·2023-07-19
Medtronic spinal implant recall due to out-of-specification device dimensions
Medtronic Catalyft LS Expandable Interbody System spinal implants are being recalled due to out-of-specification device dimensions that may affect proper placement and spinal support.
Product
Medtronic Catalyft LS Expandable Interbody System, Anterier Standalone Cage, REF 981023322, spinal implant
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0902-2023·2023-07-19
Careone Allergy Relief tablets recalled for failed impurity and degradation specifications
Careone Allergy Relief fexofenadine hydrochloride 180mg tablets are recalled nationwide for failing impurity and degradation specifications. Lot 2JE2185 with expiration date 01/24 is affected.
Product
CAREONE ALLERGY RELIEF — CAREONE ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0903-2023·2023-07-19
Allergy Relief Fexofenadine Hydrochloride Tablets Recalled for Failed Quality Specifications
CVS Pharmacy is recalling 16,200 cartons of Allergy Relief fexofenadine hydrochloride tablets nationwide due to failed impurities and degradation specifications. Stop using affected lot 2DV1925 and consult a pharmacist.
Product
Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 69842-0914-39
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2128-2023·2023-07-19
Abiomed Introducer Set Recall Due to Sidearm Detachment Risk
Abiomed 14Fr Low Profile Introducer Sets are being recalled due to silicone oil contamination that may cause sidearm detachment during use. One detachment has been documented; no injuries have been reported.
Product
Abiomed 14Fr Low Profile Introducer Set, Product Number 1000457
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0897-2023·2023-07-19
Sunmark and Generic Eye Drops Recalled for Manufacturing Deficiency
K.C. Pharmaceuticals is recalling 341,568 bottles of Sunmark and generic tetrahydrozoline eye drops due to manufacturing practice deficiencies. The recall affects multiple brands distributed nationwide.
Product
SUNMARK EYE DROPS ORIGINAL FORMULA — SUNMARK EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2023·2023-07-19
Medtronic Catalyft LS Spinal Implant Recall for Out-of-Spec Geometry
Medtronic is recalling Catalyft LS spinal implants due to potential out-of-specification device geometries that may not properly accommodate patient anatomy.
Product
Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027725, spinal implant
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0900-2023·2023-07-19
BASIC CARE Allergy Tablets Recalled Due to Failed Quality Specifications
BASIC CARE ALLERGY (fexofenadine hydrochloride) 180 mg tablets are being recalled nationwide due to failed impurities and product degradation specifications. Approximately 11,904 cartons were affected.
Product
BASIC CARE ALLERGY — BASIC CARE ALLERGY (FEXOFENADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0901-2023·2023-07-19
Berkley Jensen Allergy Relief Recalled for Failed Quality Specifications
L. Perrigo Company is recalling Berkley Jensen Allergy Relief tablets due to failed product quality specifications involving impurities and degradation. Consumers should verify their lot numbers and expiration dates.
Product
BERKLEY JENSEN ALLERGY RELIEF — BERKLEY JENSEN ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0907-2023·2023-07-19
Fexofenadine Hydrochloride Tablets Recalled for Failed Purity Specifications
L. Perrigo Company is recalling 15,504 cartons of Fexofenadine Hydrochloride 180 mg tablets nationwide due to failed impurity and degradation specifications.
Product
FEXOFENADINE HYDROCHLORIDE — FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2119-2023·2023-07-19
Medtronic Catalyft LS Spinal Implants Recalled for Out-of-Specification Dimensions
Medtronic recalls 25 units of Catalyft LS spinal implants (lot numbers NM21J039, NM21M026) due to out-of-specification device dimensions that may affect surgical fit and function.
Product
Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981025522, spinal implant
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2118-2023·2023-07-19
Medtronic Catalyft LS spinal implant recalled for out-of-specification device dimensions
Medtronic is recalling eight units of Catalyft LS Expandable Interbody System spinal implants due to potential out-of-specification device dimensions that could affect surgical fitting and spinal stability.
Product
Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981023325, spinal implant
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0916-2023·2023-07-19
Sodium Chloride Injection Bags Recalled for Potential Leakage and Sterility Risk
B. Braun Medical Inc. is recalling 79,880 bags of Sodium Chloride Injection due to potential leakage that could compromise sterility. No illnesses or injuries have been reported.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0913-2023·2023-07-19
Sunitinib Malate Capsules Recalled Due to Excess Moisture Content
Teva Pharmaceuticals is recalling 180 bottles of Sunitinib Malate Capsules due to moisture content exceeding approved specifications. The affected lot (100037220) expires 10/2024.
Product
SUNITINIB MALATE — SUNITINIB MALATE (SUNITINIB MALATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2108-2023·2023-07-19
Osteomed AutoDrive Screws Recalled for Undersized Screw Head
Osteomed recalls orthopedic AutoDrive screws used in osteotomy procedures due to undersized screw heads that could pass through the mounting plate hole, potentially affecting surgical fixation.
Product
REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only, Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0911-2023·2023-07-19
Fexofenadine Tablets Recalled for Failed Impurity and Degradation Specifications
L. Perrigo Company is recalling Picnic Fexofenadine Hydrochloride Tablets (180 mg) nationwide because the product failed impurity and degradation specifications. The affected lot is 2DR0471 with expiration date 12/23.
Product
Picnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine, 90-count cartons, Distributed by: Thirty Madison, Inc., New York, NY 10001. NDC 45 tablets: 80159-112-03
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2136-2023·2023-07-19
Medline Non-Sterile PVP Solution Mislabeled as Sterile in Ophthalmic Kits
Medline Industries is recalling 1,500 units of non-sterile PVP solution mislabeled as sterile in ophthalmic and eye surgical kits. Users may unknowingly apply non-sterile solution in eye procedures, risking infection.
Product
MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: a) OCULOPLASTY PACK, Model Number DYNJ64572A; b) EYE PACK, Model Number VAL050EEPKB
Category
Medical Device
Distribution
Distributed nationwide