State

Maine product recalls

20,364 recalls have nationwide distribution and so reach Maine. 0 additional recalls listed Maine specifically in their distribution scope.

About recalls in Maine

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 Maine 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.

14651–14675 of 20364

SevereFDA (Food)·F-0214-2023·2023-01-11
Cranberry Sweets Meltaway Recalled for Undeclared Peanut Allergen
Cranberry Sweets & More Inc is recalling Peanut Butter Meltaway chocolates mislabeled as Mint Meltaways. The product contains undeclared peanut, a major food allergen, posing risk to allergic consumers.
Product
Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read Mint Meltaways, Cranberry Sweets and more, Coos Bay, OR 97402. The back label is read Heirloom Mint Meltaways, Ingredients: Milk Chocolate (***soy lecit
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0789-2023·2023-01-11
Medical Device Test Kit Recalled Due to Storage Temperature and Time Excursions
Biomerieux Inc is recalling 14 units of the VITEK 2 REAGENT YST TEST KIT distributed nationwide because temperature and time excursions during storage may compromise the kit's performance.
Product
VITEK 2 REAGENT YST TEST KIT VTK2 20 CARDS, CATALOG 21343
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0862-2023·2023-01-11
Nephrocheck Liquid Control Reagent Recall Due to Storage Condition Violation
Biomerieux is recalling one batch of Nephrocheck Liquid Control Reagent because the product was stored outside proper temperature and time parameters, making performance unreliable.
Product
ASTUTE REAGENT NEPHROCHECK LIQUID CONTROLS KIT US, CATALOG 500013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2023·2023-01-11
Steris Biological Indicator Lot May Fail to Detect Inadequate Sterilization
Steris Corporation is recalling 338 boxes of VERIFY Dual Species Biological Indicators (Lot #230613) because some units fail to promote spore growth as intended, risking false-negative sterilization test results.
Product
VERIFY Dual Species Self-Contained Biological Indicators, 50 per box Item Number: S3060 Intended for use in installation testing and routine monitoring of steam and ethylene oxide sterilization processes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0798-2023·2023-01-11
VIDAS Listeria 60T Clinical Diagnostic Test Kit Recalled for Storage Failure
Biomerieux recalls VIDAS Listeria 60T test kits (Batch 1009371140) distributed nationwide because storage conditions were exceeded and product performance cannot be guaranteed. Users should discontinue use and contact the manufacturer.
Product
VIDAS CLINICAL VIDAS LISTERIA 60T, CATALOG 30700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0858-2023·2023-01-11
PPM Lombard TSA Neutralizer Culture Media Recalled for Storage Defect
Biomerieux is recalling 74 units of PPM Lombard Products TSA 3P neutralizer culture media due to temperature and time storage excursions. Product performance cannot be guaranteed.
Product
PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 423723
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0813-2023·2023-01-11
Culture Medium Recall Due to Temperature Excursion Affecting Product Performance
Biomerieux Inc recalls PPM INDUSTRY COMBOURG LPT BROTH culture medium batches 2117760 and 2120100 due to temperature excursion that may compromise product performance and reliability.
Product
PPM INDUSTRY COMBOURG LPT BROTH (4X3L), CATALOG 410849
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0784-2023·2023-01-11
Biomerieux API 20 E 25 Strips Recalled for Storage Condition Failure
Biomerieux Inc is recalling API 20 E 25 Strips (Batch 1009226560) because temperature and time excursions during storage exceeded specified parameters. Product performance cannot be guaranteed.
Product
API 20 E 25 STRIPS, CATALOG 20100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0835-2023·2023-01-11
VITEK 2 Antibiotic Susceptibility Test Kits Recalled Due to Storage Condition Failures
Biomerieux Inc is recalling VITEK 2 Reagent AST-GN73 test kits nationwide because they were stored outside proper temperature and time ranges, potentially compromising test accuracy.
Product
VITEK 2 REAGENT AST-GN73 TEST KIT 20 CARDS, CATALOG 413404
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0814-2023·2023-01-11
Biomerieux VITEK MS Clinical Reagent Recall Due to Temperature Excursion
Biomerieux is recalling VITEK MS-DS clinical reagent due to temperature and time conditions that exceeded specification. Thirteen units distributed nationwide cannot guarantee product performance.
Product
VITEK MS CLINICAL REAGENT VITEK MS-DS, CATALOG 410893
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0822-2023·2023-01-11
FDA Recalls ETEST Ertapenem Antibiotic Susceptibility Test Due to Storage Damage
Biomerieux Inc. is recalling ETEST Clinical Ertapenem antibiotic susceptibility test strips after temperature and time excursions compromised product performance. Affected units cannot guarantee accurate test results.
Product
ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0865-2023·2023-01-11
Biomerieux Recalls VIDAS LH 60 Clinical Tests for Temperature-Induced Performance Issues
Biomerieux is recalling VIDAS LH 60 diagnostic test kits nationwide due to temperature and time excursion. The affected batch's product performance cannot be guaranteed due to storage conditions exceeding acceptable parameters.
Product
VIDAS CLINICAL VIDAS LH 60 TESTS, CATALOG 30406-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0783-2023·2023-01-11
Listeria Detection Test Strips Recalled for Unreliable Performance
Biomerieux is recalling API Listeria detection test strips that were exposed to temperature and time exceedance during storage. Product performance cannot be guaranteed as a result.
Product
API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0831-2023·2023-01-11
ETEST Clinical Vancomycin Test Kits Recalled Due to Storage Damage
Biomerieux Inc is recalling 7 units of ETEST Clinical Vancomycin VA 256 test kits due to storage temperature excursions that may compromise test performance. Affected kits were distributed nationwide.
Product
ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0837-2023·2023-01-11
VITEK 2 Antibiotic Susceptibility Test Kits Recalled for Storage Condition Exceedance
Biomerieux is recalling VITEK 2 REAGENT AST-GN80 test kits due to temperature and time excursions during storage or handling. Product performance cannot be guaranteed for affected units.
Product
VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS, CATALOG 413437
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0792-2023·2023-01-11
VITEK 2 AST-GP67 Reagent Test Kit Recalled Due to Storage Condition Excursion
Biomerieux Inc. is recalling VITEK 2 Antibiotic Susceptibility Test Kits (AST-GP67) due to storage temperature and time conditions exceeding acceptable limits, which cannot guarantee product performance.
Product
VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0878-2023·2023-01-11
VITROS Intact PTH Reagent Pack recalled for negatively biased measurement results
Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to negatively biased measurement results (average -12% shift). The affected reagent lots were distributed worldwide and may produce inaccurate patient test results.
Product
VITROS Immunodiagnostic Products Intact PTH Reagent Pack- IVD For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum and plasma (EDTA or heparin) Catalog Number: 6802892
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0779-2023·2023-01-11
Steris Biological Indicators Recalled for Inconsistent Spore Growth
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because some units in lot 230613 fail to consistently promote spore growth, potentially masking failed sterilization cycles.
Product
VERIFY Dual Species Self-Contained Biological Indicators, 100 per box Item Number: S3061 Intended for use in installation testing and routine monitoring of steam and ethylene oxide sterilization processes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0851-2023·2023-01-11
ETEST Clinical Eravacycline ERV test kit recalled for temperature storage excursion
Biomerieux is recalling ETEST Clinical Eravacycline ERV test kits nationwide after temperature and time storage conditions exceeded acceptable ranges, making product performance unreliable.
Product
ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0857-2023·2023-01-11
VITEK 2 AST-XN09 test kit recalled for improper storage temperature and time conditions
Biomerieux is recalling VITEK 2 AST-XN09 test kits where performance cannot be guaranteed due to storage outside proper temperature and time parameters. Affected kits nationwide should not be used.
Product
VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0869-2023·2023-01-11
Medical Device Reagent Recall Due to Storage Condition Exceedance
Biomerieux is recalling DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 reagent kits because temperature and time storage conditions were exceeded, preventing performance guarantees. Distributed nationwide, affected units should be removed from service.
Product
DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 (6X1.8ML), CATALOG 306-R1026-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0846-2023·2023-01-11
ETEST Antibiotic Susceptibility Test Kit Recalled for Storage Degradation
Biomerieux Inc recalled ETEST antibiotic susceptibility test kits from batch 1009384490 due to storage conditions exceeding safe temperature and time parameters, potentially affecting test accuracy.
Product
ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0841-2023·2023-01-11
ETEST Clinical Ceftolozane/Tazobactam Antibiotic Susceptibility Test Recalled for Temperature Excursion
Biomerieux is recalling ETEST Clinical Ceftolozane/Tazobactam S30 diagnostic tests (batch 1009420460) due to storage temperature and time excursions. Product performance cannot be guaranteed, and test accuracy may be affected.
Product
ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30, CATALOG 414445
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0860-2023·2023-01-11
ETEST Vancomycin Susceptibility Test Recalled Due to Storage Damage
Biomerieux recalled ETEST vancomycin susceptibility tests after storage temperature and time excursions that may compromise product reliability and test accuracy.
Product
ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0876-2023·2023-01-11
PPM Lombard Phosphate Buffer Recall Due to Temperature Exposure
Biomerieux Inc is recalling PPM Lombard Phosphate Buffer products due to temperature and time exposure during storage or transport that may have compromised product performance.
Product
PPM LOMBARD PRODUCTS T PHOSPHATE BUFFERSTERILE 20X9ML, CATALOG T8035
Category
Medical Device
Distribution
Distributed nationwide