State

Minnesota product recalls

73,833 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,851
Critical: 1,137
Severe: 2,246
Most recent: 2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55901–55925 of 81684

ModerateFDA (Devices)·Z-0783-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMTB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0773-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMM4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0781-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMTB10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0752-2016·2016-02-17
Toshiba INFX-8000V X-Ray System Recalled for Dose Meter Error
Toshiba is recalling four INFX-8000V Bi-Plane X-Ray Interventional Systems because a software error caused dose data to be lost during specific imaging procedures.
Product
INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0576-2016·2016-02-17
Bulletproof FATwater Lemon Bottles Recalled for Microbial Growth
Bulletproof Digital Inc is recalling FATwater Lemon bottles due to microbial growth detection. No pathogens were found.
Product
FATwater bottle, 16.9 fl. oz., Lemon flavor, UPC 6 09015 50475 8
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0656-2016·2016-02-17
Fagron Recalls SyrSpend SF Suspending Base Due to Yeast Contamination
Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product contains yeast. The recall covers 88 bottles distributed nationwide.
Product
SyrSpend SF, Suspending Base, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-9.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0772-2016·2016-02-17
Zimmer Dental Implants Recalled for Missing Instructions
Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.
Product
IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0774-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Product
IMPLANT,TM, MTX 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMM4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0795-2016·2016-02-17
PharmaCaribe PulmoSal 7% Sodium Chloride Inhalation Solution Recalled for Mislabeling
Pharmacaribe LLC is recalling PulmoSal 7% Sodium Chloride inhalation solution because vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+).
Product
PharmaCaribe PulmoSal 7% Sodium chloride, Inhalation Solution, 7% Sterile, Preservative -free, Non-pyrogenic, pH 7.4 For Inhalation Only Rx Product Usage: The contents of these vials are used in conjunction with a nebulizer for the induction of sputum production where…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0575-2016·2016-02-17
Bulletproof Recalls Berry FATwater Bottles Due to Microbial Growth
Bulletproof Digital Inc is recalling 12,583 bottles of Berry FATwater due to microbial growth detection. No pathogens were detected.
Product
FATwater bottle, 16.9 fl. oz., Berry flavor, UPC 6 09015 50477 2
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0573-2016·2016-02-17
Bearded Brothers BOLD Coconut Curry Energy Bars Recalled for Mold
Bearded Brothers LLC is recalling 128 cases of BOLD Coconut Curry energy bars due to mold. The product was distributed nationwide.
Product
Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g UPC: 8-50430-00513-5.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0794-2016·2016-02-17
Merge Healthcare Recalls RadSuite Picture Archive System for Measurement Errors
Merge Healthcare is recalling RadSuite picture archive systems because they may display incorrect Standardized Uptake Values (SUV). The recall covers 164 units distributed nationwide.
Product
RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344, 5.30.3, 5.30.4, 5.30.4 HF0418E, 5.30.5, 5.30.5 HF0404E, 5.30.5 HF0413E, 5.30.5 HF390E, 5.30.5 SB0368, 5.30.6, 5.30.6 HF0405E, 5.30.6 HF0406E, 5.30.7, 5.30.7…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0780-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX FULL 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMT4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0659-2016·2016-02-17
Sandoz Recalls Candesartan Cilexetil Tablets Due to Impurity Failures
Sandoz Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because the product failed impurities and degradation specifications at a 9-month stability timepoint.
Product
Candesartan Cilexetil Tablets, 16 mg, a) 30 count (NDC 00781-5938-31) and b) 90 count (NDC 00781-5938-92) bottles, Rx Only, Manufactured by Mylan Laboratories Limited Hyderabad 500 034, India for Sandoz Inc. Princeton, NJ 08540
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0776-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc is recalling specific dental implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMMB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0577-2016·2016-02-17
Bulletproof Recalls Tangerine FATwater Bottles Due to Microbial Growth
Bulletproof Digital Inc is recalling 5,748 bottles of Tangerine FATwater due to microbial growth detection. No pathogens were detected.
Product
FATwater bottle, 16.9 fl. oz., Tangerine flavor, UPC 6 41871 93693 9
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0775-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Instructions in Manual
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because critical safety information was missing from the instruction manual.
Product
IMPLANT,TM, MTX 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMMB10 Product Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or more…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0758-2016·2016-02-17
Spectranetics Recalls Expired 2.3mm Turbo-Power Laser Atherectomy Catheters
Spectranetics Corp. is recalling 8 units of 2.3mm Turbo-Power OTW Manual laser atherectomy catheters because they are past their expiration date.
Product
2.3mm Turbo-Power OTW, Manual, Model No 423-050 Product Usage The Turbo-Power System (Laser Atherectomy Catheter) is a laser atherectomy device designed for use with the CVX-300" Excimer Laser System. The Turbo-Power Laser Atherectomy Catheter is a sterile, single use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0779-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the latest instructions for use.
Product
IMPLANT,TM, MTX FULL 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMT4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0654-2016·2016-02-17
Fagron Recalls SyrSpend SF Syrup Due to Yeast Contamination
Fagron, Inc. is recalling SyrSpend SF syrup-suspending vehicle due to the presence of yeast. The recall affects 44 bottles distributed nationwide.
Product
SyrSpend SF, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 500 mL bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-5.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0784-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific dental implants because safety information was missing from the instructions for use.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 16 mm diameter 3.5 mm Catalog #TMTB16 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0660-2016·2016-02-17
Amerisource Recalls Candesartan Cilexetil Tablets Due to Impurity Failures
Amerisource Health Services is recalling 716 cartons of Candesartan Cilexetil Tablets, 16 mg, due to failed impurities and degradation specifications.
Product
Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0782-2016·2016-02-17
Zimmer Dental Implants Recalled for Missing Instructions in Manual
Zimmer Dental Inc is recalling specific Trabecular Metal implants because the latest instruction manual omitted critical safety information for certain sizes.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMTB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0777-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Instructions
Zimmer Dental Inc. is recalling specific dental implants because important safety information was missing from the latest instruction manual.
Product
IMPLANT,TM, MTX 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMMB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V086000·2016-02-16
Starcraft AR-One Toy Hauler Recall for Incorrect Tire Labels
Starcraft is recalling 2016 AR-One toy hauler trailers because incorrect tire labels may lead to improper tire replacement, increasing crash risk.
Product
STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
Category
Vehicle
Distribution
Distributed nationwide