Recalls affecting Pennsylvania
Notices that name Pennsylvania in their distribution area, plus every nationwide recall — nationwide recalls reach Pennsylvania too.
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Class II · 4 months ago
Howmedica Osteonics Corp. TRI TS Baseplate Size 3 recall: Stryker has identified that Triathlon Universal Baseplate Size 3 (lot
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate…
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Class I · 4 months ago
Abiomed, Inc. Impella CP Set with SmartAssist. Product Codes: 1000080 recall: Exposure to the low purge pressure occurrence may result in persistent low
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Epidural Catheter KIT: 19 GA X 90 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class I · 4 months ago
Arrow International, LLC Description/REF: PI Jacc KIT: 2L 5.5 FR X 15 CM recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as CH Open Heart recall: During an internal review, Medline identified representative samples did
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include…
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as: 1) CV Draping/Basin recall: During an internal review, Medline identified representative samples did
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include…
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Class II · 4 months ago
Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire recall: Products are labeled with incorrect Use By Date
Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation…
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Class II · 4 months ago
Medtronic O-arm O2 Imaging System recall: Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as: 1) Basic Heart Pack recall: During an internal review, Medline identified representative samples did
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include…
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Class II · 4 months ago
Dabur India Limited Med Pride, Bacitracin Zinc Ointment, 500 units, 0.9g packets recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Dabur India Limited Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz tubes recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
PAI Holdings LLC VistaPharm, Kerr Insta-Char IN AN Sorbitol Base With Cherry Flavor recall: Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
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Class II · 4 months ago
Keystone Industries Pearson Quality Topical Anesthetic Gel , Mint Flavor recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Par Health USA, LLC Buprenorphine HCl, CIII, Injection, 0.3 mg/mL recall: Crystallization; identified as Buprenorphine free base
Crystallization; identified as Buprenorphine free base
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Class II · 4 months ago
Dabur India Limited Circle K, triple antibiotic ointment, Bacitracin Zinc recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Glenmark Pharmaceuticals Inc., USA Alyacen 7/7/7 recall: Failed Impurities/Degradation Specifications: This recall is being initiated
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
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Class II · 4 months ago
Dabur India Limited Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc 400 units recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class III · 4 months ago
Sandoz Inc Focalin XR 5 mg, 30 extended-release capsules per bottle recall: Labeling: Incorrect or Missing Lot and/or Exp Date
Labeling: Incorrect or Missing Lot and/or Exp Date
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Class II · 4 months ago
Dabur India Limited Med Pride, 1% Clotrimazole Antifungal Cream recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Keystone Industries safco SensiCaine-Ultra , Topical Anesthetic Gel, Strawberry Flavor recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Dabur India Limited Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Keystone Industries Dental City Topical Anesthetic GEL, Benzocaine 20% recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Keystone Industries Burkhart topical anesthetic gel, benzocaine 20 % recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Ajanta Pharma USA Inc Aripiprazole Tablets USP recall: Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.